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  • Who Qualifies to File a CPAP Lawsuit? | Philips CPAP Lawsuit Lawyer

    Who Qualifies to File a CPAP Lawsuit? | Philips CPAP Lawsuit Lawyer

    If you or a loved one suffered health consequences due to using a recalled Philips CPAP, BiPAP, or ventilator device, you may qualify to file a CPAP lawsuit. You can hire a personal injury lawyer in your area to build your case against the manufacturer and hold them liable for compensating your damages.

    In June 2021, Philips issued a CPAP machine recall, notifying consumers to cease using or consult their physicians about using specific CPAP, BiPAP, and ventilator devices it manufactured. These devices are used to treat sleep apnea and involve blowing air through tubing to keep patients breathing throughout the night. However, Philips’ first-quarter report found that sound abatement foam in the devices can degrade and cause organ damage if inhaled.

    What is a CPAP machine?

    According to Healthline, a continuous positive airway pressure (CPAP) machine is a medical device used to treat people with sleep apnea disorders, such as obstructive sleep apnea (OSA) or central sleep apnea (CSA).

    People with sleep apnea have dysfunctional sleep processes in that their throat muscles become too relaxed and prevent the flow of air during sleep. Because of this dysfunction, people with sleep apnea stop breathing momentarily at various times during their sleep cycles.

    How do CPAP machines work?

    These machines blow a continuous flow of air through tubing and into the nose and/or mouth of the user so that they do not stop breathing at any point throughout their sleeping time.

    These machines come in various styles, so some may require users to wear masks that cover both their noses and mouths, while others can connect to the nostrils alone.

    Why are Philips CPAP machines defective?

    The CPAP, BiPAP, and ventilator machines mentioned in the Philips recall include polyester polyurethane (PE-PUR) sound abatement foam. Many sleep apnea machines are loud because they continuously blow air through tubing. The PE-PUR sound abatement foam was initially meant to reduce the noise of the sleep apnea machine. However, Philips’ quarterly report found that the foam could degrade.

    With the sound abatement foam degrading, volatile organic compounds (VOCs) were released into the tubing and made individuals prone to inhaling or swallowing the chemicals. These chemicals can lead to health issues, such as liver or kidney damage, irritation in the respiratory system, and allergic reactions. Some individuals can even develop cancer because the foam particles are carcinogenic.

    Who qualifies to file a lawsuit?

    You may qualify to file a Philips CPAP lawsuit if you developed an injury or illness as a result of using one of the company’s recalled sleep apnea devices. That means people who used recalled BiPAP or mechanical ventilators may also qualify to pursue compensation, as CPAP devices were not the only sleep apnea machines found to contain dangerous foam chemicals.

    The following factors may indicate whether you qualify to file a lawsuit:

    If you used a recalled Philips CPAP, BiPAP, or ventilator machine

    If you used any of the following recalled Philips CPAP, BiPAP, or ventilator machines and suffered health consequences, you may have grounds to file a lawsuit against the manufacturer:

    • DreamStation ASV
    • DreamStation CPAP, Auto CPAP, BiPAP
    • DreamStation ST, AVAPS
    • DreamStation GO CPAP, APAP
    • A Series BiPAP A30 and A40
    • A Series BiPAP Hybrid A30
    • A Series BiPAP V30 Auto
    • Trilogy 100 and 200
    • C Series ASV
    • C Series S/T and AVAPS
    • OmniLab Advanced Plus (In-Lab Titration Device)
    • Dorma 400 CPAP and 500 CPAP
    • SystemOne ASV4
    • SystemOne (Q-Series)
    • E30 (Emergency Use Authorization)
    • REMStar SE Auto CPAP
    • Garbin Plus, Aeries, LifeVent

    These devices were manufactured before April 26, 2021, with some models being discontinued. Philips has created newer models that do not rely on PE-PUR sound abatement foam and offers a repair and replacement program for those who wish to replace the recalled device for a safer model.

    If you suffered side effects as a result of exposure to PE-PUR foam chemicals

    The U.S. Food and Drug Administration (FDA) released a Class I recall about the Philips medical devices and warned the public about potential health risks associated with the devices. You may qualify to file for compensation if you used a recalled Philips medical device and suffered one or more of the following side effects:

    • Irritation in the nose, throat, and other parts of the respiratory tract (e.g., lungs)
    • Irritation on the skin in areas that made contact with the PE-PUR foam (e.g., eyes and mouth)
    • Headaches and migraines
    • Dyspnea, which is a condition where patients have difficulty breathing
    • Coughing
    • Nausea or vomiting
    • Inflammation and other autoimmune system reactions
    • Asthma or other breathing conditions
    • Allergic reaction
    • Dizziness
    • Chest pain
    • Symptoms of cancer

    If you exhibit any of these symptoms, please consult your physician to determine whether you have other options to treat your sleep apnea.

    If you wish to join a mass tort action against Philips for a recalled CPAP device

    The FDA released an update on the Philips recall notice in November 2021, indicating that people should still keep caution. The administration stated that they received over 3000 medical device reports (MDRs) about foam degradation and provided instructions on filing a complaint about your recalled device.

    Since the recall, victims can file individual product liability lawsuits against Philips or join a mass tort action with other victims who share similar experiences. If you are interested in joining a mass tort or multidistrict litigation (MDL) action, you can consult a law firm in your state. A lawyer may review your case and help you take legal steps to join the action.

    Can I file a CPAP lawsuit?

    Depending on when you discovered your injury or illness and its potential ties to a recalled Philips sleep apnea machine, you may still be able to file a CPAP lawsuit. Each state has a statute of limitations that details how long individuals have to file a lawsuit about a personal injury, which also applies to product liability cases (cases filed against manufacturers, designers, and marketers for releasing defective products to the public).

    Another statute to be aware of is the statute of repose, which establishes a cut-off deadline for legal actions. This may alter an individual’s ability to file a product liability suit if the specified filing period has elapsed. If you decide to work with a lawyer, they can identify whether you are still within legal time limits to file your CPAP lawsuit.

    CPAP lawsuits allege cancer risk linked to Philips devices

    The New York Times issued a report on several victims who allege the recalled Philips devices are linked to cancer, based on the medical data presented by the FDA and chemical components of the sound abatement foam. At the time of the report, August 2021, concerns about the Delta variant of coronavirus were conflicting with the demands of supplying ventilators to COVID-19 patients and patients with defective Philips’ products. Still, patients are expected to have their devices replaced.

    Some victims reported having kidney and liver damage as a result of swallowing PE-PUR foam particles. Other patients remain nervous about continuing use until they receive a replacement, with one patient expressing frustration at continuing using their device despite the health risks.

    Qualifying cancers and injuries

    You may qualify to file a CPAP lawsuit if you used a recalled Philips device and developed any of the following cancers:

    • Lung cancer
    • Kidney cancer
    • Liver cancer

    Other serious health issues like heart problems or respiratory failure can also qualify you for a lawsuit.

    CPAP lawsuits allegations

    In general, most CPAP lawsuit allegations involve the following points:

    • Philips’ negligently released defective sleep apnea machines to the public market.
    • Philips knew about the foam degradation because of its quarterly report in April but did not issue a recall until June 2021, after the release of new DreamStation models that do not contain the PE-PUR foam. Other evidence of this point includes 2015 email exchanges with Philips’ foam supplier.
    • Philips initiated a repair and replacement program in an effort to provide safer models to patients. However, the FDA withdrew its approval for the replacement machines after new reports showed that the silicone replacement foam may also have health risks (investigation pending).

    Who is eligible for a CPAP lawsuit?

    You are eligible to file a CPAP lawsuit if:

    • You own or use a Philips’ CPAP, BiPAP, or ventilator medical device.
    • You suffered injuries or developed an illness, such as cancer, after using the Philips’ device.
    • You can prove the Philips’ sleep apnea machine shows signs of foam degradation, meaning you may have inhaled or swallowed PE-PUR foam during your sleep.
    • You suffered other damages as a result of the health issues the Philips medical device caused.

    If you are still unsure whether you qualify for a lawsuit, you can get a free case review with a personal law firm that handles product liability cases. Many law firms answer basic questions in the first consultation at no charge.

    Why file a lawsuit?

    If you were a victim of one of Philips’ defective sleep apnea devices, filing a CPAP lawsuit can serve as a route to claim compensation and recover some of the damages you’ve faced.

    Do I need a lawyer to file a CPAP recall claim?

    You are not obligated to retain a lawyer to file a CPAP recall claim. However, if you are not familiar with the personal injury or product liability claims or litigation process, you may put yourself in a vulnerable position since the defendant will likely have a team of attorneys representing them. Corporate lawyers know how to use the law to their client’s advantage and will not be afraid to use your legal inexperience against you.

    Rather than risk jeopardizing your case, you can work with a personal injury lawyer who works for a contingency fee. They can build your case for you and stand up against Philips’ attorneys on your behalf to pursue compensation.

    What can a personal injury lawyer do to help me build my CPAP lawsuit?

    Your Philips CPAP lawsuit attorney can provide several services to put your CPAP recall claim together. Some services may involve:

    • Conducting an investigation into your case to identify whether it’s possible to prove that a Philips-brand sleep apnea machine caused your injury or illness
    • Contacting medical professionals who treated your condition or who can testify on your behalf to show how the PE-PUR foam inside the devices led to your health issues and to explain other potential health risks you now face
    • Gathering other forms of evidence to support aspects of your case, such as medical records, the defective medical device, and financial documents that can prove the value of specific damages you claim
    • Calculating your financial damages and estimating a value for your physical and emotional damages
    • Speaking with the defendant’s legal team, the insurance company, or court officials on your behalf
    • Preparing legal paperwork for your case and monitoring your case’s deadline so that you submit your lawsuit within your state’s statute of limitations
    • Attending negotiation meetings to organize a settlement deal, which may occur during the claims process or out of court to avoid a trial verdict

    If it becomes necessary to take your case to court, a defective product attorney can also serve as your legal representative and present your case in front of a jury to petition for your compensation. Throughout your legal journey, your legal team will provide counsel and advise you on decisions. Should you disagree with your attorney, you can elect a different option or cease work with your attorney.

    How much does a CPAP lawsuit lawyer cost?

    The cost of a personal injury lawyer’s services can vary on how long it takes to build a client’s case, what services are necessary to do so, and whether the client’s case goes to trial. So, there is no flat fee for hiring an injury attorney. However, many personal injury law firms throughout the United States work on a contingency-fee basis to allow clients to afford their services.

    As are many people’s cases, being inundated with medical treatment costs or losing employment because of your health can deplete your financial accounts. If you are worried about whether you can afford a lawyer, you don’t have to be with a contingent agreement.

    What is a contingency fee?

    A contingency fee refers to the mutual agreement between the attorney and client that the attorney will not charge their legal fees if they do not successfully win their client’s case. Within this fee agreement, the law firm may also agree to:

    • Postpone all attorney’s fees until the end of the client’s case, provided they win compensation for their client
    • Collect their fees once the client can collect their compensation
    • Use a percentage rate instead of an hourly rate to charge for their services
    • Use an agreed-upon percentage of the client’s case earnings to pay for the attorney’s fees

    You will be able to discuss these terms in full and see specific rate numbers when speaking with a team representative of the law firm. Additionally, if you do discuss your case in your first free consultation, you are not obligated to work with the law firm if you do not agree to the rates they demand for their services.

    Meet your legal team to start building your CPAP lawsuit

    If you or a loved one wants to file a personal injury lawsuit about the injuries or illness you developed after using a defective Philips CPAP machine, we can direct you to a lawyer in your area who handles CPAP lawsuits. Several law firms throughout the United States have begun building cases against the sleep apnea machine manufacturer to hold them liable for causing patients’ health problems. You can begin your legal journey by working with a lawyer in your state.

    Fill out our contact form today for help with your case or to learn about how to bring the manufacturer to account.

  • FDA Studies and Recalls Regarding Zantac | The Sentinel Group

    FDA Studies and Recalls Regarding Zantac | The Sentinel Group

    You or a member of your family may have purchased over-the-counter Zantac or been prescribed Zantac for painful and persistent acid reflux, ulcers, or heartburn. If you took this medication and were subsequently diagnosed with specific types of cancer, you could be entitled to financial compensation from the drug manufacturer. In addition to the listed ailments, you may have used it to treat other medical conditions.

    Our network of mass tort lawsuit attorneys is preparing lawsuits to help consumers and patients who took this dangerous drug get the monetary award they deserve. When you and other injured patients pursue financial compensation, we help you document your Zantac-related health care concerns, understand the drug’s harmful ingredient, and assign a financial value to your injuries. These can include medical care, lost wages, pain and suffering, and wrongful death damages, where applicable.

    Why are Zantac lawsuits being filed?

    When you take a recommended or prescribed medication, you have the right to be made aware of all possible side effects it may cause. Doctors who prescribed Zantac and consumers who used the over-the-counter version were not made aware of its dangers. When taken in high enough doses, Zantac has been found to contain NDMA in higher levels that might pose a risk of cancer in its consumers.

    According to MedlinePlus research, ranitidine—a main component of Zantac—has been identified as a possible human carcinogen (known to cause cancer). Food and Drug Administration (FDA) officials issued a recall for Zantac in its prescription and over-the-counter formulations. FDA recommendations include:

    • Consumers are advised to stop taking the medication, properly dispose of any remaining doses, and identify alternative treatment options.
    • Patients who were prescribed the drug are advised to talk to their health care provider for assistance making alternative treatment options.

    Both parties are advised to safely dispose of any remaining medications at home rather than returning them to a drug take back location. If the drug injured you or someone you love, our attorney network could help you identify ways to seek compensation from the drug manufacturer. 

    Status of Zantac lawsuits

    With legal help and support, consumers and patients have started to hold the manufacturer of Zantac responsible for its cancer-causing ingredient, ranitidine. These individuals and their families are preparing and filing lawsuits seeking monetary compensation for economic and non-economic damages. 

    Lawyers are still collecting evidence, identifying potential plaintiffs, and gathering evidence to support their clients’ requests for financial compensation. Lawyers are also preparing and organizing evidence that proves Zantac’s manufacturer was aware of the potential danger of exposure to ranitidine and did not notify prescribers, sellers, or patients. 

    Many individual Zantac lawsuits are being combined into class action and mass tort cases where multiple plaintiffs with similar legal issues are seeking compensation from a shared defendant. 

    • There have been 828 Zantac lawsuits filed in federal courts, according to United States Judicial Panel on Multidistrict Litigation records.
    • Many Zantac lawsuits are still in the preparation phase and are expected to go to trial by the end of 2022.
    • A federal judge recently dismissed cases filed against the makers of Zantac’s generic equivalent.

    We are committed to seeking compensation for anyone whose health was negatively impacted by the use of brand name Zantac products. Our network of attorneys helps patients seek compensation for their medical bills linked to cancer after using Zantac. Your compensation can also include additional expenses for lost income, pain and suffering, and more.

    Zantac class actions

    A class action lawsuit is one in which all injured parties (known as plaintiffs) request recoverable damages from the same responsible party (known as the defendant). In a class action case, each plaintiff shares equally in any resulting monetary recovery. In Zantac cases, the shared complaint points to the potential of its heartburn medication to cause cancer when stored at higher than room temperatures.

    According to an MDPIA study, prolonged use of Zantac may contribute to the following types of cancer:

    • Liver
    • Gallbladder
    • Stomach
    • Colorectal
    • Esophagus
    • Pancreatic
    • Small intestine

    If you or someone you love received a cancer diagnosis after taking any form of Zantac, our Zantac lawsuit attorneys could help you explore your compensation options. We will also help you understand the Zantac class action lawsuit options available in your area. Our lawyers will handle the details of the case, including collecting evidence that supports your right to compensation. 

    Has there been a Zantac settlement?

    As of today’s date, there have not been any Zantac lawsuit settlements, though many cases are pending. Cases involving Zantac are still in their early phases, and our attorneys are gathering evidence of the harm its users endured (and continue to endure). When settlements are negotiated recoverable damages for injured parties can include:

    • Current and future medical bills
    • Current and future income loss
    • Loss of future earning capacity
    • Physical pain and suffering
    • Mental and emotional distress

    In addition, we help you recover the funeral and burial expenses of a loved one who succumbed to an illness or disease that can be attributed to their use of ranitidine drugs (which includes Zantac). Where possible, we will also request compensation for punitive damages typically awarded in cases where the at-fault party’s actions were deemed intentional or egregious.

    When drug manufacturers fail to provide health care professionals and consumers with a transparent knowledge of the drug’s risks and dangers, consumers are entitled to pursue financial damages. This is what is happening all over the country — consumers are working with our attorney network to hold manufacturers accountable for their actions.

    How liability law applies to the Zantac cases

    Zantac lawsuits assert that the prescription ranitidine drug could be contaminated with N-nitrosodimethylamine (NDMA). According to Healthline research, NDMA is a known human carcinogen. After the FDA performed extensive drug evaluation and research, it recalled products with NDMA contamination because their risk of harm increases over time.

    Liability laws apply to Zantac cases because their manufacturer is responsible for providing reasonable care for the product’s users. They are liable for your resulting financial damages when they fail to do so by not informing you of potential hazards.

    In a statement published in 2019, Janet Woodcock, director of FDA’s Center for Drug Evaluation and Research, acknowledged the danger of NMDAs in Zantac. Product manufacturers — including drug makers — must ensure their products function as described and provide their touted benefits. 

    Product manufacturers have an equal responsibility to inform consumers of any risks or dangers inherent to the use of their products. Our network of attorneys is gathering proof that the manufacturer of Zantac knew their product contained NMDA in the form of ranitidine. Having access to this knowledge and failing to warn prescribers and patients of it constitutes negligence and financial liability on the manufacturer’s part. 

    How do I know if I have a Zantac cancer claim?

    In September 2019, FDA officials began alerting health care professionals and the patients they serve that the recall process had begun for prescription and OTC Zantac. Our attorney network helps people who took this product to treat heartburn and other troubling conditions prepare a case against the manufacturer. 

    We will help you compile your prescription receipts, retail receipts, and other evidence of your purchase of Zantac. Our team will also compile medical records and other evidence of medical harm for each client we represent. The evidence we collect will prove your right to compensation by establishing:

    • Your use of Zantac
    • Your subsequent cancer diagnosis
    • A correlation between the two 

    While you undergo, cope with, or recover from cancer treatments, our Zantac lawsuit attorneys work hard to prepare your case for the upcoming settlement or trial process. We carefully review your evidence and inform you of your right to compensation. Our lawyers will also handle the settlement negotiation process and trial procedures, depending on how your case resolves. 

    We will also explain the multi-plaintiff cases we are building and your role in it, and take care of all case-related communication and information requests. Our team will also provide regular and timely updates on the progress of your case.

    Confirm that you took Zantac

    Ranitidine medications like Zantac have led to adverse health conditions and cancer development in patients like you. If you took this medication and were later diagnosed, our attorneys could help you fight for compensation. 

    The first step to finding out if you have a case against the makers of Zantac is to contact one of our team members and see if you qualify for a free legal consultation. Our team will help prove you took Zantac by obtaining your:

    • Written diagnosis
    • Medical records
    • Medical bills
    • Prescription records
    • Prescription receipts
    • Retail receipts
    • Other records and evidence that help prove you took the drug, when you took it, and for what period

    You must have taken the name brand Zantac, not a generic form since recent court procedures dismissed claims against generic manufacturers. Brand name manufacturers of Zantac include:

    • Novartis/Sandoz
    • Apotex
    • Pfizer
    • GlaxoSmithKline
    • Sanofi
    • Boehringer 
    • Others

    The records we collect on your behalf will prove:

    • Which version or versions of Zantac you took
    • Which manufacturer made the Zantac you took
    • Whether you took the drug in pill or liquid form

    We handle the evidence collection part of your case for you to focus on your current and future health.

    Confirm that you regularly used Zantac for a significant amount of time

    Part of the FDA, the Center For Drug Evaluation (CDER), works vigilantly to ensure everyday consumers receive safe and effective drugs. They oversee and regulate OTC and prescription drugs, among other substances. 

    At first thought safe and effective, the prescription and OTC versions of Zantac were typically prescribed or recommended to treat:

    • Stomach ulcers
    • Intestinal ulcers
    • Pain and discomfort
    • Heartburn
    • Acid reflux
    • Painful indigestion

    If you or someone you love took Zantac to treat or prevent ulcer pain or other medical conditions, your use might have been short- or long-term. Our attorney network will obtain copies of the following evidence to prove you took Zantac for a significant amount of time:

    • Health care records
    • Doctor’s notes
    • Laboratory test results
    • Pharmacy records
    • Pharmacy receipts
    • Retail receipts
    • Pill bottles
    • Medication packaging

    Our team may also take statements and testimonials from you and any family members or in-home assistants who provided you with ongoing care. We obtain these records on your behalf, whenever possible, to ensure your evidence file points to your use of Zantac for an extended time.

    Confirm related diagnoses

    You could be eligible to join other injured parties in a class action or mass torts lawsuit. You or someone you love will have to have received a diagnosis of cancer from unacceptable levels of NDMA affecting any of the following areas, among others:

    • Liver
    • Gallbladder
    • Stomach
    • Colorectal
    • Esophagus
    • Pancreas
    • Small intestine

    Your medical records, testimony from the physician treating your cancer, and your future prognosis are all forms of evidence that will help us. Our team must prove your cancer diagnosis is related to your use of Zantac. In addition to cancer, other illnesses that might be related to Zantac and, therefore, entitle you to compensation include:

    In addition to the medical evidence and documents listed above, our team members may also request confirmation of your diagnosis, proof of the extent of your Zantac usage, and records that document your medical history. We will also ask questions about any other adverse reactions to Zantac you may be experiencing. 

    Contact an attorney to discuss your options

    Were you or someone you love diagnosed with cancer after taking prescription or OTC ranitidine medication branded as Zantac? Our network of attorneys at The Sentinel Group can help you seek financial compensation for your medical bills and related expenses. 

    Fill out our contact form today for help with your case.

  • Surgical Staples Lawsuit | Free Case Evaluations | 24/7 Service

    Surgical Staples Lawsuit | Free Case Evaluations | 24/7 Service

    On March 8, 2019, the U.S. Food & Drug Administration (FDA) released a letter to healthcare providers describing 41,000 safety issue reports the agency received about surgical staples.

    In the letter, the FDA noted that between 2011 and 2018, surgical staple errors resulted in 366 deaths, 9,000 serious injuries, and over 32,000 other forms of malfunctions. As a result, many lawsuits are unfolding against the makers of these devices, citing that because they released unsafe products into the market, they owe injured claimants compensation.

    The bottom line: If you or a loved one suffered harm because of surgical staples, you can pursue a lawsuit against the liable parties. Financial recovery in your case could account for medical bills, lost income, and pain and suffering.

    Key takeaways from surgical staple lawsuits

    Here are some key details about surgical staple lawsuits at a glance:

    • Plaintiffs claim that some of the nation’s top surgical staple producers knowingly allowed dangerous products to harm patients.
    • More than 56,000 adverse events were reported to the FDA regarding surgical staples. However, this information was not made public for years afterward, per Kaiser Health News.
    • In 2015, a landmark case secured an $80 million verdict for an injured claimant who suffered life-threatening conditions after receiving surgical staples. After further investigation, Ethicon was found responsible for its defective product.
    • Since then, claimants have filed individual lawsuits against various surgical staple manufacturers.
    • With the help of a lawyer from our network, you can hold these parties accountable for harming you or your loved one.

    What are surgical staples?

    Surgical staples are exactly what they sound like: staples. They are sometimes used in place of sutures or stitches and are usually made out of stainless steel or high-grade plastic.

    Per Healthline, surgical staples don’t dissolve in the body during the healing process as stitches are designed to do. However, there are several benefits of surgical staples, including:

    • They reduce surgery time.
    • They tend to heal more effectively and reduce scarring.
    • They can be less painful than alternatives.

    For years, surgical staples have served as vital resources for surgeons and other healthcare practitioners. However, as more information becomes available, it appears that some staple brands have done more harm than good.

    What are surgical staples used for?

    Surgical staples are sometimes seen as a better alternative to stitches or sutures. They are also used for complex wound or incision closures, per Healthline.

    They may be used in procedures such as:

    • C-sections
    • Gastrointestinal operations
    • Gynecologic surgery
    • Thoracic surgery
    • And more

    In an ideal situation, these mechanisms close complicated wounds and allow for speedy recovery times. In less-than-ideal situations, these staples lead to life-threatening complications.

    What is the case against Ethicon and other surgical staples manufacturers?

    Let’s get one thing out of the way first. The pending lawsuits regarding surgical staples aren’t against the mechanisms themselves. Instead, they’re against the makers of these defective products.

    These lawsuits allege that certain companies that produced surgical staples knew about the products’ potential harm but failed to notify the public. As a result, countless people suffered severe injuries, life-threatening infections, and other dire health consequences.

    Many lawsuits are against two companies named Ethicon and Medtronic. They’re two of the largest surgical staple manufacturers in the U.S., and they make 80% of every stapler used in American hospitals.

    Surgical staples lawsuits have led to settlements

    In 2012, retired police officer Florence Kuhlmann underwent a surgery that involved surgical staples. After complaining of stomach pain and discomfort, doctors found that her bowels had been stapled to her rectal wall, rupturing her bowels. In the end, a judge and jury awarded $9.8 million in compensatory damages and $70 million in punitive damages.

    Her lawsuit hinged on one important fact: because Ethicon (the defendant) knew about its product’s propensity for harm but failed to issue a recall or notify the public, it should be held responsible. Since then, many lawsuits have alleged similar wrongdoings.

    What health effects did people suffer?

    According to the FDA, defective surgical staplers have led to the following health conditions:

    • Sepsis (also known as “blood poisoning”)
    • Organ perforation
    • Fistulas (the abnormal connection of two body parts or organs)
    • Organ and tissue tears
    • Increased risk of secondary health conditions, like cancer
    • Internal bleeding
    • Life-threatening complications and death

    Ethicon and other companies are responsible for surgical staple errors

    Ethicon and Medtronic aren’t the only companies responsible for issuing defective products. The following organizations are also involved:

    • Reach Surgical
    • Meril Life
    • U.S. Surgical Corporation
    • Welfare Medical
    • Zimmer Biomet
    • CONMED
    • 3M
    • Cardica
    • CareFusion Corporation
    • Frankenman International
    • Stryker
    • Smith & Nephew
    • Purple Surgical

    Surgical staples have undergone many recalls in the last decade

    The FDA has issued dozens of recalls on surgical staples, dating back to 2003. Still, this did not dissuade product manufacturers from allowing these items to reach consumers. Ethicon’s surgical staple product recall was categorized as a Class I recall, meaning that these products could seriously harm consumers.

    How do you know if surgical staples caused your losses?

    After any kind of procedure, whether it involves surgical staples or not, you should be aware of certain complications. You should report any concerns to your doctor so they can better examine your condition. Some indicators of surgical staple complications include:

    • Bruising around the incision site
    • Swelling
    • Discoloration
    • Pus or blood oozing from the surgical site
    • Pain or disconcerting numbness
    • A change in your bodily functions (like whether you can have a bowel movement)
    • Fainting or lightheadedness
    • Infection
    • Heat around the surgical site
    • The wound reopening

    If you experience any of these signs, go to the emergency room or schedule an appointment with your doctor. The longer you wait to seek a professional opinion, the more at risk your health.

    You may qualify for legal action if the following apply to you

    Right now, you may wonder if you qualify to file a lawsuit against a surgical staple manufacturer. If you can answer “yes” to one or more of the following questions, you may have a valid case:

    • Did you undergo an operation or procedure that involved surgical staples?
    • Did those surgical staples directly cause health complications?
    • Did you suffer financial, physical, and emotional losses?
    • Did the manufacturer of the surgical staples know (or should have known) about a possible danger?

    If you’re not sure whether you qualify to pursue compensation, consider utilizing our network of attorneys. We connect injured claimants to qualified product liability lawyers with experience in product liability cases. These individuals can evaluate your circumstances and determine your recourse options.

    You can recover these damages through a surgical staples lawsuit

    The value of your losses depends on the specifics of your situation, including:

    • The extent of the injury
    • Whether you lost a loved one or suffer a permanent disability
    • The value of your financial losses (such as medical bills, lost income, and more)
    • Your emotional health and other consequences to your life

    Compensable losses in your case may include the following:

    Economic damages related to your financial losses

    After suffering harm or losing a loved one to a surgical staples injury, economic damages in your case could comprise:

    • Medical bills. You can seek the cost of surgical repairs, hospitalization, and cosmetic surgery. These costs may extend well into the future, depending on the severity of your injury.
    • Lost income. Your settlement or court award may include the cost of your lost wages, bonuses, tips, commissions, and employee benefits (like insurance).
    • Loss of future earning capacity. Surgical staple errors can cause lifelong disabilities that prevent you from working full-time or even at all. Compensation in your case could cover your lost future wages and inability to work.
    • Assistive devices. This includes the cost of wheelchairs, crutches, drains, colostomy bags, and in-home modifications.

    Non-economic damages, or those pertaining to your non-financial hardships

    The law allows injured claimants to seek damages for more than financial losses. It also allows claimants to seek compensation for the physical and emotional ways their injuries have affected them. Non-economic damages in your case may include:

    • Disability. A botched surgery can have lifelong implications on your mobility, ability to live independently, and mental health. Your settlement can account for the way the error affected your day-to-day function.
    • Pain and suffering. This expense compensates you for your physical pain and emotional suffering. It’s calculated based on the circumstances of your situation, like your mental health and missed time from work.
    • Disfigurement. Many healthcare providers use surgical staples because they minimize the risk of scarring. When these products malfunction, however, they can completely alter one’s appearance.
    • Loss of enjoyment of life. If you’re unable to partake in activities you once enjoyed, pursue your career, or otherwise live a full life, you can seek compensation for this hardship.

    Punitive damages, or those intended to punish the defendant

    Earlier, we mentioned that in the case of Kuhlmann v. Ethicon Endo-Surgery LLC, the plaintiff secured $70 million in punitive damages. These damages were not intended to cover the victim’s financial losses. Rather, they were intended to punish the negligent party — in this case, Ethicon.

    Punitive damages are seldom awarded in personal injury cases. However, this legal precedent suggests that in these cases, punitive damages are a possibility.

    How long do I have to file my lawsuit?

    How long you have to file your lawsuit depends on many factors unique to your situation. While many of these lawsuits are against the makers of defective surgical staples, some of them also accuse healthcare providers of performing subpar procedures.

    Basically:

    • The statute of limitations in your case depends on where you live. Some states give you a year to file your lawsuit while others allow for more leniency.
    • Some states allow for the “discovery” rule. This would give you additional time from the date you discovered your condition to file.
    • The nature of your case also dictates your legal deadline. Product liability and medical malpractice cases sometimes come with different filing rules and timeframes.
    • If you’re filing on behalf of a late loved one, different deadlines may apply. The statute of limitations generally begins from the date of your injury or when you discovered it. However, for wrongful death lawsuits, your filing deadline begins from the day of your loved one’s passing.

    It’s important to understand your case’s statutory deadline

    The statute of limitations is one of the most important laws surrounding your case. Why?

    • Failing to file your case on time could jeopardize it. If the court sees that you filed outside of the applicable deadline, they could dismiss your case with prejudice. This would prevent you from filing it again––even if additional details come to light.
    • If the courts dismiss your case, the other party has no obligation to offer compensation. The financial burden of your injuries could fall solely to you.

    Connecting with a lawyer from our network is one way to protect your legal rights. They can determine your case’s deadline and take action accordingly.

    How can a lawyer from our network help you seek compensation?

    Major corporations sometimes go to great lengths to protect their interests. After learning about your case, they may send you pushy messages or even have their lawyers talk you into dropping the lawsuit.

    Your legal representative can stand between you and these entities. You can expect your legal team to do the following:

    A lawyer will gather evidence to prove your case

    Your lawsuit alone will not yield compensation. You need supporting information to assert the cause of your injuries and the cost of your damages.

    Supporting information to demonstrate these facts could include:

    • Imaging scans
    • Testimony from your doctor, family members, and yourself
    • Information from the FDA about the product
    • The treatments needed to address the problem
    • Your medical bills, income statements, and other injury-related receipts
    • Photos of the surgical site
    • The names of your medications
    • Your loved one’s death certificate and cause of death (if you’re filing a wrongful death lawsuit)

    A lawyer will consult with field experts on your case

    The above information alone may not compel a judge and jury to award damages. Your lawsuit lawyer may consult with industry experts regarding various aspects of your situation, including your damages, health condition, and mental state.

    Some of these specialists may include:

    • Healthcare professionals, like doctors, nurses, professors, and surgeons
    • Mental health professionals
    • Economists

    These professionals’ insight can reveal important facts about your financial losses, pain and suffering, and overall situation.

    A lawyer can calculate the value of your losses

    It’s important to know the true value of your damages. With this goal figure in mind, you can seek compensation that fully covers the cost of your injury-related losses. In addition to consulting with industry experts, your lawyers may use the following forms of evidence to calculate your losses:

    • Employment records
    • Wage statements
    • Medical bills
    • Physical therapy invoices
    • Receipts from necessary medical equipment
    • Your personal testimony

    A lawyer will attempt to negotiate a settlement

    Kuhlmann v. Ethicon Endo-Surgery LLC set a legal precedent for these types of cases. Now that surgical staple manufacturers know they’re possibly liable for victims’ injuries, they may offer out-of-court settlements.

    If negotiating a settlement is not an option, your lawyer can pursue a verdict at trial in order to seek compensation.

    A lawyer will manage your lawsuit

    Product liability lawsuits are admittedly complicated. Dealing with cases involving major medical device makers requires substantial evidence and preparation. To help your civil case, your representative can:

    • File your case in the appropriate jurisdiction
    • Prepare you to give a statement
    • Take depositions
    • Present your case’s evidence
    • Request the full scope of your damages from the liable party
    • Manage and abide by all courtroom procedures
    • Object to any unfair proceedings
    • Communicate with the involved parties
    • Guide your case through to a verdict

    After filing your case, the liable party may offer a settlement. If this amount covers your losses, you can avoid a trial.

    You could pay nothing out-of-pocket for legal aid

    Many of the lawyers in our network work on a contingency-fee basis. In this arrangement, these firms finance their clients’ cases — which can include everything from consulting to filing fees.

    When an attorney takes your case, you can expect to:

    • Partake in a free case review about your damages, circumstances, and health condition
    • Agree to your lawyer’s terms of payment in writing
    • Have a lawyer set your case in motion without paying anything upfront
    • Have a portion of your potential settlement go toward your attorney’s fees
    • Pay nothing if your lawyer doesn’t “win” your lawsuit

    Now is the time to consider your legal options and hold these malicious corporations responsible –– not worrying about affording legal aid.

    Commonly asked questions about surgical staple lawsuits

    We know that you want to have the “big picture” before you connect with a lawyer from our network. Right now, we can provide answers to some of these most commonly-asked questions:

    What is the average settlement for a surgical staple case?

    There’s no data available to answer this question. The outcomes of private insurance negotiations are not always available to the public.

    However, you should know that the value of your specific case will depend on your age, health condition, and financial losses.

    Can I file a case on behalf of an injured or late loved one?

    This depends on where you live. Every state has different rules regarding who can file lawsuits on behalf of others.

    In general, if your child suffered harm due to surgical staples, you can file a lawsuit on their behalf. If you lost a loved one, however, this again depends on where you live.

    While some family members can initiate legal action, other states dictate that only “personal representatives” can do so. These entities can be named by the courts or in a decedent’s will.

    How long does it take to resolve a product liability lawsuit?

    Lawsuits of this nature can take time to resolve — sometimes, several years. The progression of a case depends on a lot of factors, including the evidence to support the case and whether or not the defendant is willing to negotiate an out-of-court settlement.

    Your lawyer’s job isn’t just to secure compensation for your losses — it’s also to keep your case moving forward. Remember: if you’re represented on a contingency-fee basis, your lawyer’s paycheck rides on your case’s success.

    If you don’t recover compensation, they don’t recover compensation for their help. This provides them an extra incentive to advance your lawsuit.

    What do I need to prove in my surgical staples case?

    In civil cases involving car accidents (for example), you have to prove negligence, meaning that someone acted without regard for others’ safety. However, your case is different. That’s because in product liability cases, you don’t prove negligence. Instead, your evidence must assert:

    • You (or a loved one) underwent a procedure that involved surgical staples.
    • The surgical staples’ manufacturer knew (or should have known) about the possibility of harm, but did not recall the product or warn healthcare providers.
    • You suffered harm or lost a loved one.

    If your legal team can prove these three things, then you could secure compensation for your injury-related expenses.

    About our services

    We’re not a law firm. We’re a lawyer referral service. Our number one goal is to connect injured claimants to legal resources. Our directory is filled with board-certified, trial-ready lawyers who handle medical device lawsuits against major corporations and other related matters.

    Here’s what you can expect from us:

    Learn if you qualify

    We encourage all prospective clients to fill out our online evaluation form. Here, we’ll ask for the following:

    • Your name
    • Address, including the city, zip code, and state
    • Your phone number
    • Your email address
    • A brief description of your situation

    While describing your case, be sure to include as many details as possible. We want to know about the details of your surgery, when you discovered your condition, and what financial losses you incurred.

    Help from our nationally recognized referral service

    We’re not just any legal referral service. We take pride in helping injured people. Some of our memberships include:

    • We’re one of the founding members of the Mass Torts Vendor Association. Our vision is to provide outstanding service with dignity and respect for claimants’ needs.
    • We’re also part of the Mass Torts Vendor Association’s Advisory Working Committee. We frequently provide insight to the Committee about what practices can enhance our clients’ experiences.
    • We belong to The National Trial Lawyers, an invitation-only organization that includes some of the nation’s primer attorneys.

    With our experience, we work to connect people who’ve been injured with excellent legal assistance.

    A free case review with a surgical staples lawsuit lawyer

    Many of the lawyers in our directory offer free case reviews. This allows you to describe your situation to a legal professional who can assess your situation and explain your options. If you don’t connect with a lawyer or their firm, no problem; these consultations come with no obligation.

    Fill out a free case evaluation form now

    Ready to learn more about moving forward with a surgical staples lawsuit? Fill out our case evaluation form now. We’ll be in contact as soon as we review your situation’s details. Remember: the statute of limitations in your case is ticking, so prompt action is of the essence.

    Related Links

    What Causes Surgical Staples Injury?
    What Money Damages can Surgical Stapling Victims Recover?
    Who is Eligible to File a Surgical Staples Lawsuit?
    Money Damages Surgical Stapling Injuries
    Are Surgical Staples Safe?
    Surgical Staples Lawsuit Eligibility

  • Paraquat Lawsuit & Parkinson’s Disease | Seek Recovery for Your Injuries

    Paraquat Lawsuit & Parkinson’s Disease | Seek Recovery for Your Injuries

    In recent years, scientific studies have found a link between paraquat dichloride and a higher risk of developing Parkinson’s disease. While ingestion of this toxic chemical is widely known to be fatal, these studies suggest that repetitive exposure to commercial herbicides containing paraquat could have long-term health consequences. As a result, several countries have banned or restricted its use. 

    Many people have also come forward with lawsuits against the biggest paraquat manufacturers, demanding compensation for their or their loved one’s health conditions. If you or your family member was exposed to paraquat and later received a diagnosis for Parkinson’s, kidney failure, or other illnesses, you could seek compensation through a paraquat lawsuit. Our team can connect you with legal representation. 

    What is paraquat?

    Paraquat dichloride is a highly toxic chemical that appears in multiple commercial herbicides. Farmers and agricultural workers most commonly use paraquat as a weed killer and desiccant to protect a variety of crops leading up to harvest season, though it is also frequently used for grass control. 

    It is not to be confused with Roundup—another popular herbicide currently under legal fire—which contains the toxic chemical glyphosate. In fact, paraquat’s growing popularity is often attributed to the fact that weeds have become resistant to glyphosate products.

    While many herbicide products contain paraquat as an active ingredient, the most widely known brand in the United States is Gramoxone. It’s currently produced by Syngenta, the main company now facing lawsuits for adverse health conditions allegedly connected to paraquat exposure, including Parkinson’s disease. Other brands known to contain this agrochemical include, but are not limited to:

    • Parazone
    • Helmquat 3SL
    • Firestorm
    • Quick-Quat
    • Para-Shot 3.0
    • Crisquat

    According to the Centers for Disease Control and Prevention (CDC), paraquat was first introduced for herbicide use in the early 1960s, though scientists had identified the chemical long before that. Since then, it has become the most popular herbicide in the United States. 

    Meanwhile, dozens of countries have banned its use in recent years, including Japan, Thailand, Brazil, China, the United Kingdom, and, more broadly, the European Union. Most notably, Switzerland—where Syngenta is headquartered—also prohibits the use of paraquat products. 

    Despite these bans and the rising number of legal cases related to its use, the United Kingdom and Switzerland both continue to export the chemical for sale to farmers and agricultural workers all over the world, including the United States. As reported by the BBC, the U.K. exported more than 28,185 tons of pesticides containing paraquat in 2018 alone, with 14 tons marked for U.S. sale. 

    Is paraquat safe?

    All parties agree that paraquat is acutely toxic to both humans and animals with improper use or ingestion. According to a toxicity summary of paraquat from the Wireless Information System for Emergency Responders (WISER), repeated skin exposure can cause skin and eye irritation. However, disagreements lie in whether use of the chemical causes long-term health issues even when proper precautions are taken. 

    Defenders of paraquat argue that the most risk involves accidental or intentional ingestion. Inhalation and prolonged skin exposure to large amounts of paraquat can also lead to paraquat poisoning, which is why this chemical is under strict regulation. 

    Paraquat safety in the U.S.

    Due to the extreme toxicity of paraquat, the U.S. Environmental Protection Agency (EPA) has set strict safety requirements for its use. Namely, the agency has labeled paraquat a restricted use pesticide (RUP), meaning only certified applicators can use it; it is not approved for residential use. Training is necessary before one can receive certification.

    In addition, there are numerous safety policies to follow during application. Herbicides containing paraquat are generally available in liquid form and sprayed on crops by aircraft. It is believed that health risks fall significantly once the application area has dried. For this reason, the EPA advises users to: 

    • Limit the number of acres sprayed per applicator per day
    • Avoid spraying when non-certified workers are present or may come into contact with the chemical before it dries
    • Wear and maintain personal protective equipment (PPE) to prevent inhalation
    • Discard clothing that becomes heavily contaminated
    • Read and follow safety labels carefully
    • Avoid storing paraquat in any food or drink containers
    • Avoid using or storing the chemical near residential areas or other high-traffic locations 
    • Apply the chemical using the largest droplet setting possible for the highest level of spray control

    Despite these precautions and regulations, many parties have come forward, claiming illness after being exposed to paraquat. Even those who live near farmland where paraquat herbicides are used could be at risk of adverse health effects due to spray drift

    It’s also worth noting that these regulations have not always been in place. For example, the EPA only established its mandatory training requirements for paraquat herbicide use in 2016. 

    Paraquat exposure in local communities

    EPA safety documents have acknowledged the occurrence of spray drift during the application of paraquat products. Spray drift refers to when the wind carries herbicide droplets to areas not intended for contact. To determine the risk of spray drift occurring and spreading toxic chemicals to nearby communities, scientists regularly model aerial pesticide application.

    For example, a study published in Atmospheric Environment outlines the results of one such test conducted in Washington State. The study revealed that, despite following application guidelines, spray drift carried the testing substance across a nearby residential area. 

    While this study did not involve paraquat specifically, it suggests that similar scenarios are possible with any herbicide applied in this way, potentially leading to exposure in local communities.

    The CDC suggests that licensed applicators are the most at-risk due to repeated proximity to the chemical. However, other parties who could suffer exposure to paraquat include:

    • Other agricultural workers and farmers
    • Those who live or work in communities close to farms that use paraquat
    • Licensed applicators’ close family members 

    Aside from exposure due to aerial pesticide application, the CDC cites ingestion as the most common danger associated with paraquat. Ingestion of any amount of this chemical can lead to immediate paraquat poisoning.

    What is paraquat poisoning?

    Paraquat poisoning occurs from the intentional or accidental ingestion of paraquat. Unfortunately, herbicides containing this chemical have been linked to many cases of suicide and attempted suicide because of their high toxicity. Even more alarming are the numerous reports of accidental poisonings due to improper storage. 

    The EPA issues strict warnings about storing any herbicides in food or beverage containers, as others may unknowingly consume the toxic chemicals. As a precaution, Paraquat manufacturers include colored dyes, sharp odors, and emetics—substances used to induce vomiting—in their formulations. 

    Even so, the EPA has recorded several instances of accidental paraquat ingestion, including in more recent years. In response, the agency established new packaging requirements to further protect against poisoning in 2016. This includes a closed-packaged system to prevent:

    • Pouring the chemical into other containers
    • Spills
    • Mixing the chemical with food or beverage

    Paraquat dichloride facts and figures

    The EPA’s updated policies and ongoing review of paraquat use were largely in response to the alarming number of poisonings reported from accidental ingestion. Specifically, the California Poison Control System and American Association of Poison Control Centers (AAPCC) reached out to the EPA about a series of fatal paraquat poisonings in San Joaquin Valley in 2013. In letters to the EPA, these agencies cited the following statistics:

    • There were 50 deaths related to paraquat ingestion.
    • Of those deaths, 12 were traced to paraquat that was being stored in a drink container.

    More broadly, studies such as this one in Yonsei Medical Journal estimate that roughly 20 deaths per million worldwide are attributed to paraquat.

    Paraquat dichloride: the toxicity of a single sip

    The Hazardous Substances Data Bank (HSDB) entry on paraquat reports that a lethal dose is estimated at 14mL of a 40% solution of the chemical depending on body weight. As 14mL equates to just under three teaspoons, this has led many to conclude that a single sip of paraquat is enough to cause death.

    There is currently no known antidote for paraquat poisoning, according to MedlinePlus and other sources. Doctors can focus only on alleviating the symptoms and addressing any complications as they occur. 

    Paraquat poisoning symptoms vary based on the type of exposure

    Though a single sip of paraquat can be fatal due to the absence of an antidote, the exact symptoms experienced depend on the amount ingested. Regardless of the level of exposure, it is critical to seek medical attention as soon as possible. While the presence of the emetic should immediately induce vomiting, this can quickly lead to deadly levels of dehydration. 

    Receiving rapid medical care could be life-saving. It will allow doctors to take additional steps to remove the paraquat from the victim’s system and provide IV fluids to maintain safe hydration levels. 

    According to the CDC, some symptoms of paraquat poisoning are immediate, while others may develop in the hours, days, or weeks after. For example, victims typically experience painful swelling in the mouth and throat right away, followed by nausea, abdominal pain, diarrhea, and vomiting as the emetic takes effect. Other potential symptoms for different levels of ingestion are outlined below.

    Ingestion of small or medium amount

    Those who consume a few drops or sips worth of paraquat dichloride could experience scarring on the lungs, as well as multiple types of organ failure, particularly involving the:

    • Kidney
    • Liver
    • Heart

    Ingestion of large amount

    Those who consume a larger amount of paraquat experience the symptoms outlined above at an accelerated rate. Other potential symptoms include:

    • Confusion
    • Muscle weakness
    • Seizures
    • Coma
    • Fluid in the lungs
    • Respiratory failure

    Inhalation 

    Inhaling toxic herbicides like paraquat can significantly damage the airways and lungs, including scarring. This may develop over a period of several weeks and can make breathing and swallowing difficult for victims. 

    Excessive skin exposure

    Paraquat poisoning can also occur through contact with the skin in the following situations:

    • Prolonged exposure
    • Concentrated exposure (Paraquat herbicides are typically diluted with water before application.)
    • Exposure to broken skin

    Potential symptoms include:

    • Blistering or burns
    • Loss of fingernails
    • Mouth ulcers
    • Nosebleeds
    • Blindness

    Note: The symptoms outlined in the sections above are not limited to paraquat poisoning—they could suggest other types of illness or poisoning. Nevertheless, you are advised to seek immediate medical attention for yourself or a loved one if there is a risk of severe dehydration or other potentially fatal conditions. 

    Paraquat poisoning side effects 

    While it is possible under certain circumstances to survive paraquat poisoning, victims are likely to suffer lingering and even long-term side effects. This typically includes:

    • Permanent scarring of the airways and lungs
    • Organ failure

    Several studies have also indicated a connection between long-term exposure to paraquat and an increased risk of developing Parkinson’s disease.

    How is paraquat linked to Parkinson’s disease?

    The high toxicity and widespread use of herbicides containing paraquat have led many to question whether there are any long-term effects of exposure—particularly for agricultural workers who use the product regularly and communities in proximity. 

    The emergence of multiple studies conducted on this topic in recent years has caused many to question their or their loved one’s diagnoses and deaths. This includes instances of Parkinson’s disease in individuals who suffered varying amounts of paraquat exposure. 

    Studies suggest chronic paraquat exposure increases the risk of Parkinson’s disease

    Many scientific studies—like this one in Environmental Health Perspectives—assert there is a connection between exposure to this chemical and the eventual diagnosis of Parkinson’s. However, the EPA has yet to take steps to ban paraquat use in response due to the currently conflicting nature of science on this subject. 

    The agency reviewed the available literature and performed a draft risk assessment on paraquat in 2019. As a result of this assessment, the EPA concluded there is not a clear enough link at present between paraquat and Parkinson’s disease.

    Not much is known about the overall cause of Parkinson’s disease, and issues with exposure assessment make it difficult to study the potential connection with paraquat. Still, many researchers believe the chemical’s toxic properties can create conditions for Parkinson’s in the brain.

    How paraquat may create conditions for Parkinson’s disease

    As Mayo Clinic explains, Parkinson’s disease is associated with nerve cell damage in the brain, specifically related to the cells that create dopamine. Such damage causes a drop in dopamine levels, leading to abnormal brain function. Associated symptoms include:

    • Tremors
    • Muscle rigidity and slowed movement, including chewing
    • Difficulty keeping balance and walking
    • Loss of unconscious, automatic movements, such as swallowing and blinking
    • Speech and cognitive impairment
    • Issues with bladder control
    • Emotional changes
    • Sleep disorders

    According to the study in Environmental Health Perspectives, the reason researchers relate paraquat exposure with Parkinson’s is that its neurotoxic properties cause oxidative stress in the brain, resulting in a similar loss of dopamine-producing neurons.

    Syngenta denies a connection between paraquat poisoning and Parkinson’s

    According to Syngenta, 377 other companies currently sell paraquat products around the world, and more than 42 million farmers have relied on it to protect vital crops like soy and cotton. 

    The agrochemical producer denies there is any link between paraquat and Parkinson’s disease and insists it has followed all laws in the countries where it manufactures and sells Gramoxone. Further, Syngenta asserts it has taken appropriate steps to minimize the risk of accidental ingestion through its use of emetics and blue dye in the herbicide.

    Still, this has not stopped numerous farmers and other individuals from coming forward to sue the company. Multiple lawsuits have been initiated and are in the beginning stages as of September 2021.

    Paraquat lawsuits are already underway

    Several parties began filing lawsuits against paraquat manufacturer Syngenta in early 2021. This quickly escalated to a class action lawsuit in Iowa (Holliday v. Syngenta AG et al.) However, as dozens of claims began popping up in California and other states, the decision was made to file multidistrict litigation (MDL).

    The MDL was filed on June 7, 2021, in the U.S. District Court for the Southern District of Illinois. In addition to Syngenta, the MDL also names Chevron, which maintained a license to produce and sell Gramoxone for several decades.

    Known as Paraquat Products Liability Litigation MDL No. 3004, the MDL initially consolidated 14 cases, with at least 77 potentially related cases. However, Bloomberg reports that as many as 400 cases have come forward this year, and many more are expected. 

    The report also points out that Syngenta has already initiated steps to settle certain cases, offering $187 million. Still, a jury trial has been scheduled for November 15, 2022. 

    You could qualify to join current paraquat litigation

    After an MDL consolidates a number of cases, a few are chosen to represent the rest in the initial stages of litigation. These are known as bellwether cases, which serve as examples of what other claimants can expect if their lawsuits move forward. Based on the proceedings’ jury rulings in the bellwether cases, defendants may feel pressured to settle to avoid additional cases. 

    MDL No. 3004 has only just gotten started—the first of the bellwether cases are not set to begin until late 2022, meaning there is still time for you to join. However, your time to sue is still subject to the statute of limitations, so it is crucial not to wait if you plan to seek damages. This filing deadline depends on the type of case you are filing and other factors, which your attorney can help you navigate as soon as you request their services.

    Filing a lawsuit against paraquat manufacturers

    If you or a loved one received a Parkinson’s diagnosis or experienced other negative health effects after exposure to paraquat herbicides, you have legal options. With a class action and MDL already underway, you may be able to join your case with many others who claim similar experiences. 

    By filing a paraquat lawsuit, you have a chance to hold manufacturers like Syngenta responsible for the harm their products caused. You could recover compensation for various expenses and losses, as well as pain and suffering that you and your family experienced as a result of the paraquat-related diagnosis. Bringing attention to the problem could also encourage the EPA and other agencies to take further action and prevent others from suffering similar injuries or illnesses. 

    In any defective product case, you could recover compensation for various damages. Some may be economic, related to the expenses and losses you suffered due to your or your loved one’s injuries. Others are meant to address non-economic damages related to the intangible harm the defective product caused. 

    For example, in a paraquat lawsuit regarding a Parkinson’s diagnosis for your loved one, you could seek compensation for the following:

    • Doctor’s visits
    • Neurological examinations and brain scans
    • Medications to control Parkinson’s symptoms
    • Medical devices
    • The cost of ongoing care to handle your loved one’s daily needs
    • Pain and suffering
    • Funeral costs and related expenses if you lost your loved one due to Parkinson’s

    These are just examples—the damages you qualify to recover will depend on the specifics of your case and the type of lawsuit you file. 

    Hiring a paraquat lawyer

    Defective products cases against major manufacturers are often overwhelming, time-consuming, and difficult to navigate. These cases grow even more complex when they involve multiple manufacturers operating on a global scale. That’s why many victims of defective products band together to form MDLs and class actions. 

    They also hire attorneys familiar with handling these massive cases to represent them. You do not have to build a paraquat lawsuit and fight Syngenta and other herbicide manufacturers on your own. Our team can connect you with the right law firm for your case.

    How a defective product attorney can support claim

    When you hire a law firm to represent you in paraquat litigation, your paraquat lawsuit attorney will handle all legal matters for you. They will:

    • Advise you on your legal options and help you make decisions throughout the process
    • Compile the evidence available to support your claims
    • Calculate the damages your or your loved one’s paraquat-related injuries caused
    • Represent you in all case proceedings
    • Work with experts who can provide support
    • Take steps to help you join the current MDL or class action, if appropriate
    • Advocate for your financial recovery, whether through receipt of a settlement or court award

    It’s worth noting that many personal injury firms offer free consultations regarding cases like these. Many defective product attorneys also work for a contingency fee, so there is no need to worry about your ability to afford legal representation. In a contingency fee arrangement, clients pay nothing unless they receive compensation, and attorney’s fees come out of whatever they recover. 

    Choosing the best law firm for your paraquat case

    Though there is little to no financial risk when you hire a contingency fee law firm, you still want to ensure you’re choosing a legal team you can trust. This means doing some research and asking the right questions during the initial consultation. Personal injury firms generally offer this first consultation for free for this exact reason—it gives you a chance to learn about their services and approach to cases like yours. 

    Here are a few questions to consider before hiring a firm to represent you in paraquat litigation:

    • Does the firm have a positive reputation in the community? (You can use Google reviews, peer reviews, and other sources to verify this.)
    • How many defective product cases has the firm handled? 
    • Does the firm have a track record of securing settlements and court awards?
    • Will the firm handle cases that may join an MDL or class action?
    • How accessible will your attorney be if you have questions about the case?
    • What are the specifics of the firm’s fee arrangement?
    • What specific services does the firm provide?

    It can take some time to find the law firm best suited for your case. However, our team is here to help.

    Reach out for legal help with your paraquat lawsuit

    Others have already initiated the steps for holding paraquat manufacturers like Syngenta responsible for harm they suffered. You have a chance to join them, seeking justice and compensation for your or your loved one’s diagnosis after exposure to this toxic chemical herbicide. 

    Global manufacturers should not get away with creating and distributing harmful products that even preventative measures cannot protect against. Your first step toward justice could be hiring a law firm to handle the rest of the legal process for you. Our team is here to assist you.

    Fill out our contact form to get help with your case or to learn more about how you can bring the the manufacturer to account.

    Related Links

    What are Paraquat Settlements?
    Paraquat Poisoning Lawsuit Status
    All About Paraquat Settlements
    Does Paraquat Cause Parkinson’s Disease?
    What You Need to Know About Paraquat & Parkinson’s Disease

  • 3M Earplugs Lawsuit | Hearing Loss, Tinnitus Claims

    3M Earplugs Lawsuit | Hearing Loss, Tinnitus Claims

    If you used earplugs manufactured by 3M while serving in the military and suffered a severe hearing impairment, you may be eligible to file a 3M earplugs lawsuit. You may qualify to receive a settlement to compensate you for the losses related to your damaged hearing. Time limits do apply to these cases, so finding out if you qualify for legal relief right away can be critical to your case.

    There is no risk or cost to you to determine whether you or a loved one qualifies for compensation. You can learn more about the eligibility requirements for the 3M earplugs lawsuit and what steps to take next if you meet those requirements. This process may allow you to get compensation for your hearing loss, tinnitus, or other hearing-related damage.

    What is the problem with the 3M military earplugs?

    From 2003 to 2015, 3M annually provided about 15,000 packages of earplugs to the military. Each package contained 50 sets of earplugs. Over a 12-year-period, that amounts to nine million pairs of earplugs — all of which had defects that 3M knew about and chose to conceal.

    The shortened stems on the 3M Combat Arms earplugs caused the earplugs not to fit properly in the ears of some service members.

    This poor fit also caused the earplugs to slowly loosen from the ear canal and even fall out altogether. These ill-fitting earplugs obviously could not perform their essential function of safeguarding the hearing of soldiers.

    Legal help for injured soldiers

    When people suffer injuries from using a consumer product, they may have a legal claim against the product designer, manufacturer, and distributor, among others. Companies have a legal duty to develop products that are safe for consumer use. When they fail to do so, injured parties may have a product liability claim against those companies.

    Similarly, the allegations that 3M furnished defective earplugs to the U.S. government for use by the military forms the basis for a product liability claim.

    Discovery of internal 3M documents revealed during these lawsuits shows that 3M had knowledge of the defects in the earplugs yet failed to advise the military of the defects. For instance, although 3M had tested the earplugs for safety while being worn in one configuration, service members were instructed to use them in a different configuration.

    Injured soldiers claim that 3M knew that their earplugs were defective and would not protect the hearing of military personnel. Nonetheless, 3M moved ahead with its exclusive U.S. government contract, which caused the distribution of defective earplugs to thousands of service members.

    If you or a loved one meets all the eligibility requirements, you may have a product liability claim against 3M. You may qualify to receive compensation for your hearing loss or tinnitus due to the failure of the 3M earplugs to protect your hearing. By getting legal advice about your situation, you can determine whether you are eligible for this form of legal relief.

    3M earplug lawsuit verdicts

    Two trials have resulted in large verdicts for the plaintiffs, or the injured soldiers who filed suit:

    • On May 9, 2021, a federal jury in Florida awarded $7.1 million to three servicemen who suffered hearing loss after using 3M earplugs. The verdict included $2.1 million in punitive damages.
    • On June 7, 2021, a Florida jury awarded a soldier $1.7 million in damages, but found him to be 38% at fault, therefore reducing his award to $1.1 million.

    3M agreed to a settlement in the False Claims Act lawsuit

    In 2015, soldiers began recognizing the defects in the 3M dual-ended combat arms earplugs, and the federal government terminated its exclusive contract with 3M for the earplugs. Next, in 2016, a private party acting as whistleblower for the federal government took legal action against 3M by filing suit under the False Claims Act.

    This federal law makes companies, who are usually federal government contractors, liable for defrauding the U.S. government.

    The whistleblower claimed in its lawsuit that 3M was aware of the defects in the 3M earplugs that would cause them to be less effective than represented. They alleged that 3M took the following actions when it entered an exclusive contract with the U.S. government to provide the military with the defective earplugs:

    • 3M knew the earplugs were defective and would not perform as intended
    • 3M failed to disclose the defect in the earplugs
    • 3M hid or falsified test results that would have revealed the defect

    Ultimately, 3M agreed to settle the False Claims Act lawsuit by paying the federal government $9.1 million. 3M also had to pay the whistleblower $1,911,000. However, the settlement did not require 3M to admit that it had committed any wrongdoing in the matter.

    In other words, it did not admit to any of the allegations in the lawsuit regarding the earplugs.

    Value of a 3M earplug lawsuit

    The value of a 3M earplug lawsuit is unknown. Various factors can influence the settlement in mass tort lawsuits like those involving the 3M earplugs, and many factors are still unknown. As more trials go forward and jury verdicts result, you are likely to have a better sense of the outcome of any settlement in these cases.

    You might also wonder about paying for legal representation in your 3M earplug lawsuit. Most law firms take these types of cases on a contingent-fee basis. As a result, you pay no legal fees up front to get started on your case.

    In fact, you pay no legal fees while your case is going on. You pay legal fees only when there has been a settlement or jury verdict at the resolution of your case. Paying legal fees should never be a barrier for injury victims to seek justice and compensation for their injuries through the legal system.

    Who is eligible to file 3M earplug lawsuits?

    You may be eligible to file a 3M earplug lawsuit if you meet the following conditions:

    • You served in any branch of the U.S. military.
    • Your military service occurred from 2003 to 2015.
    • You used the dual-sided 3M Combat Arms earplugs.
    • You were exposed to loud sounds during your military service.
    • You suffered hearing loss or tinnitus during your military service.

    You can be either a U.S. veteran or a current U.S. military member and still be eligible to file a claim against 3M. However, if you are currently serving in the military, you must ensure that your hearing loss or tinnitus is well documented in your medical records.

    Disability status and eligibility to file suit

    Some individuals who have suffered hearing loss or tinnitus are disabled by their injuries. As a result, they may receive full or partial VA disability benefits. Your VA disability rating, however, does not determine whether you are eligible to file a lawsuit against 3M.

    Even if you have a zero disability rating, your hearing loss or tinnitus may still have a significant negative impact on your life. You still may be eligible to seek compensation from 3M for your hearing problems if you meet all other eligibility criteria.

    Dual-ended combat arms earplugs were too short

    3M contracted with the U.S. government to design, manufacture, and provide special ear protection for all four branches of the U.S. military. The dual-sided 3M Combat Arms earplugs were specially made to allow soldiers to adjust and optimize hearing under different conditions in combat zones, as follows:

    • One side allowed soldiers to totally block very high-level, loud noises.
    • The other side allowed soldiers to still be able to hear low-level, quieter sounds that were nearby with limited interruptions, such as verbal commands, while blocking out more damaging sounds.

    The stems on the earplugs ultimately proved to be too short for the ears of soldiers. This problem led to the soldiers being unable to properly insert the earplugs. Additionally, the earplugs eventually would loosen and work their way out of their ears, therefore failing to block the damaging sounds as intended.

    The Combat Arms earplugs that 3M produced originally were too large to fit into the earplug carrying case that accompanied them, making it inconvenient for soldiers to carry them. The earplugs also interfered with helmets fitting correctly for some soldiers. These problems caused 3M to shorten the stems of the combat earplugs.

    Shortening the stems of the earplugs caused even larger problems for thousands of service members using them. The earplug stems were not long enough to properly fit into the ears of some soldiers. The earplugs also could loosen slightly during wearing, thus weakening the high-level hearing protection that they were supposed to provide.

    In some cases, the military earplugs fell out altogether. In other cases, the earplugs became loose enough to break the airtight seal meant to keep sound out. Ultimately, usage of the earplugs led to hearing loss and tinnitus for many soldiers that they could have avoided by using earplugs that were not defective.

    3M’s military earplugs caused hearing loss in servicemembers

    Aearo Technologies originally developed Combat Arms earplugs, which were specially designed to protect the hearing of U.S. service members in all branches of the military. 3M purchased Aearo in 2008, along with the exclusive contract with the U.S. government to provide earplugs to the military. 3M is therefore responsible for the defects in the earplugs, both before and after its purchase of Aearo in 2008.

    The earplugs were defective in that they failed to protect the soldiers from hearing loss as intended. Soldiers in war zones often experience high-decibel noises that cause hearing loss and related damages, such as:

    • Gunfire
    • Explosives
    • Aircraft
    • Artillery

    Repeated exposure to these loud noises leads to permanent hearing loss, tinnitus or ringing in the ears, and other hearing-related problems. To avoid these problems, the U.S. included 3M combat earplugs as standard equipment hearing protection for every soldier in all four military branches. Despite the best efforts of the U.S. government to protect the military, 3M knowingly provided the military with a defective product that caused harm to thousands of soldiers.

    Soldiers face lifelong hearing loss

    According to the U.S. Department of Veterans Affairs (VA), hearing problems, including hearing loss and tinnitus, is by far the most common service-related disability among U.S. veterans. An estimated 1.3 million veterans receive disability compensation from the VA for hearing loss, and another 2.3 million veterans receive disability compensation from the VA for tinnitus.

    It is especially common among military service members who served in combat zones, such as:

    • Iraq
    • Afghanistan
    • Somalia
    • Syria
    • Libya

    Some veterans with hearing loss may benefit from surgery, medication, or implants. However, other former military personnel have permanent hearing loss that hearing aids may help, but not eliminate.

    Hearing problems also can lead to problems with speech. Auditory processing disorder, in which veterans can pass hearing tests but have a hard time understanding speech, also can result from hearing damage from military service.

    The Veterans Administration (VA) regularly treats veterans for hearing loss, tinnitus, and more. Veterans may receive VA disability benefits in part or in full due to their hearing problems. The consequences of hearing loss can be permanent and devastating.

    Service members are at a risk of hearing loss as a part of their duties, which is why the federal government furnished them with special earplugs. 3M knew the defective earplugs did not work, and knowingly put service members at risk. Due to the potential severity of hearing loss and the purposely harmful conduct of 3M, the damages that you may receive from an earplug lawsuit against 3M could be significant.

    What is the value of a 3M military earplugs lawsuit?

    The settlement in any hearing loss case, including the 3M combat earplug cases, varies widely from one case to the next. Hearing loss and other damages are not insignificant. Individuals may be unable to continue serving in the military due to hearing loss or unable to work in other careers after discharge from the military.

    Some of the other factors that may impact a settlement in a personal injury case involving hearing loss may include:

    • The extent and severity of the hearing loss or damage
    • The impact of the hearing loss or damage on your ability to work
    • The ability to successfully treat your hearing loss or damage
    • The permanency of the hearing loss or damage

    While some treatments, implants, or hearing aid devices may improve hearing loss or damage, hearing loss ultimately is permanent. As a result, settlement values must reflect the permanency of the injuries, which likely would be higher than a settlement value of a temporary or curable injury. However, every case is different, so the settlement offer that one individual receives may be higher or lower than what another individual receives.

    The importance of getting treatment for hearing loss

    Hearing loss or tinnitus is the kind of disability or impairment that is not immediately apparent to others. While others can easily tell that a person who cannot walk or who is missing a limb is disabled, it is not so easy to demonstrate hearing loss and related damages. So, soldiers affected by hearing loss and related issues must have medical documentation of their impairments.

    Getting medical treatment for their hearing problems can be crucial to proving eligibility for compensation in a 3M earplugs lawsuit. Without concrete medical proof, jurors may assume that you are able to function normally without any problems, despite your claimed disability. This is just one example of the type of evidence that is necessary to present in this type of lawsuit.

    Likewise, you must provide evidence showing how your hearing loss, tinnitus, or auditory processing disorder affects your daily life. You can explain the details as to how the impairment affects you, both personally and professionally.

    For instance, your hearing loss may make it impossible for you to continue serving in the military, and also may make you unable to work in some other occupations.

    Next steps in the 3M earplug lawsuits

    The next 3M earplug lawsuit is scheduled for trial on September 22, 2021. The following trial is scheduled for November 2021. Meanwhile, the judge handling the multidistrict litigation (MDL) in Florida federal district court has scheduled an additional six cases for trial on dates ranging from November 2021 to February 2022.

    Furthermore, the judge has identified the first “wave” of MDL cases to be moved to the active docket of the court. As a result, about 1,500 of the over 250,000 pending cases will receive deadlines and hearing dates as their parties prepare for trial. Subsequent waves of MDL cases could include as many as 20,000 cases.

    Meanwhile, another 1,000 cases are still pending in state court in Minnesota. These cases, too, are likely to start going to trial. Therefore, 3M will have trial dates coming up soon in both federal and state court.

    The pressure on the 3M company to settle the earplug lawsuits continues to build for a variety of reasons. The reasons that may make a settlement more imminent include:

    • The 3M earplug suits make up the largest mass tort MDL in history.
    • The judge handling the MDL is aggressively moving thousands of cases to the active court docket and setting trial dates.
    • More bellwether cases are scheduled for trial in the next few months.
    • Four out of five soldiers have won substantial jury verdicts against 3M in the suits that have gone to trial so far.

    No one can predict how or when 3M will start settling cases. As pressure from all directions continues, however, settlement becomes more and more likely. Only time will tell how long it takes for a settlement to finally occur.

    Learn more about your eligibility for compensation in a 3M earplug lawsuit

    If you or a loved one suffered hearing loss or tinnitus after serving in the military between 2003 and 2015, you may have fallen victim to the defective 3M combat earplugs.

    You may be able to pursue a 3M earplugs lawsuit and seek compensation for your injuries. Fill out our contact form today for help with your case or to learn how you can hold the manufacturer accountable.

    Related Links

    3M Earplug Lawsuit Average Payout
    Has Anyone Received Money from a 3M Earplug Lawsuit?
    What Was The Defect In The 3M Earplugs
    How do you qualify for a 3M military earplug lawsuit?
    What Law Firm Is Handling the 3M Earplug Lawsuit?

  • Movement seen in Philips CPAP lawsuits as cases are consolidated in MDL

    Movement seen in Philips CPAP lawsuits as cases are consolidated in MDL

    On October 8, 2021, the Judicial Panel on Multidistrict Litigation (JPML), which comprises seven circuit and district judges, ruled to consolidate lawsuits filed against Philips Respironics, the maker of recalled continuous positive airway pressure (CPAP) and other respiratory devices.

    Reuters reported the news, along with the fact that Senior U.S. District Judge Joy Flowers Conti will oversee the pretrial and discovery hearings for the lawsuits under MDL No. 3014 – In Re: Philips Recalled CPAP, Bi−Level PAP, and Mechanical Ventilator Products Liability Litigation.

    Why the Philips CPAP lawsuits are being consolidated

    To date, hundreds of claimants have taken legal action against Philips. The lawsuits center on the DreamStation product line of devices’ defective sound-abatement foam. This component of the DreamStation devices allegedly breaks down and/or off-gases, causing users to ingest or inhale toxic or carcinogenic substances and become ill.

    The cases share common questions of fact, making them suitable for consolidation in multidistrict litigation (MDL). The purpose of MDL is to streamline the judicial process in similar cases by conserving resources and facilitating consistency across a large number of lawsuits. Typically, the judge who manages an MDL encourages plaintiffs and defendants to agree on a settlement.

    Under the MDL, the Philips cases in which evidence points to consistent questions of fact have been transferred to a single court, the United States District Court Western District of Pennsylvania. Most of Philips’ recalled devices were manufactured outside Pittsburgh, making it the logical choice for hosting pretrial hearings, according to the JPML.

    Story of the plaintiff who asked for the MDL

    Plaintiff Thomas Starner filed a motion for the consolidation of the Philips cases. Starner’s lawsuit states that he purchased a Philips Respironics Remstar Pro CPAP in 2013 and used it every night up to April 2018. The plaintiff then bought a Philips DreamStation Auto CPAP device, which he used on a nightly basis until June 26, 2021. On this date, Starner was notified of the recall of both devices because of the dangerous PE-PUR foam.

    The plaintiff claims he incurred “substantial expenses” to replace the recalled devices. Furthermore, according to the complaint, Starner has endured “chest tightness and respiratory irritants” while using the Philips devices. News of the recall allegedly has caused Starner to suffer anxiety about his health due to the possibility that he ingested or inhaled dangerous substances from the machines.

    How will the MDL play out for Philips CPAP lawsuit plaintiffs?

    The federal court judge will manage the pretrial and discovery process. During discovery, both sides of the lawsuits will depose witnesses, exchange documents, and issue interrogatories. During this process, individual lawsuits could be either dismissed or settled. Those that are neither dismissed nor settled will be sent back to their state courts for trial.

    In other words, each Philips case will be decided on its own merits. Only the discovery and pretrial hearings are shared across the various lawsuits.

    CPAP repair plan expected to complete in one year

    Philips reported that its CPAP repair and replacement program is “underway.” According to the company, it has built approximately 750,000 replacement devices and repair kits. Although more than 250,000 of these units have been delivered to customers, Philips anticipates that only in a year’s time will all users have received their replacement devices and repair kits.

    The U.S. Food and Drug Administration (FDA) announced the recall of millions of Philips Bi-Level Positive Airway Pressure (Bi-Level PAP), Continuous Positive Airway Pressure (CPAP), and mechanical ventilator devices in June 2021. The agency labeled the recall as a Class I recall, a classification reserved for the most serious recalls of products that could cause serious injuries or death.

    Fill out our contact form to learn how you can hold the manufacturer liable if you suffered injuries.

  • AFFF – Firefighter foam lawsuit

    AFFF – Firefighter foam lawsuit

    For decades, Aqueous Film Forming Foam (AFFF) has been used by military personnel, firefighters, and airport workers to put out liquid fires. Because AFFF has toxic chemicals and carcinogens, exposure to the product can lead to cancer and other health complications. The manufacturing companies knew the health risks involved with this product and refused to speak up and warn users.

    If you or a family member incurred an illness due to AFFF exposure, you might be entitled to pursue compensation for your related losses. The Sentinel Group can connect you with a law firm that can manage your case and file an AFFF lawsuit while you focus on getting the treatment you need.

    What is in AFFF?

    According to the Environmental Protection Agency (EPA), AFFF is made up of per- and polyfluoroalkyl substances (PFAS), which are man-made, produced in high quantities, and cannot break down naturally. Perfluorooctane sulfonate (PFOS) and perfluorooctanoic acid (PFOA) are two types of PFAS that are present in AFFF. In addition, they are the most commonly studied and used PFAS in the United States. 

    Because they consist of eight carbon chains, they can easily repel water and oil. Since AFFF has a high concentration of PFOA and PFOS, it is very effective in extinguishing liquid fires in chemical plants, oil refineries, offshore platforms, and airports.

    However, PFOA has been identified as Class 2B, meaning it can be “possibly carcinogenic to humans,” as the American Cancer Society (ACS) explains. As such, these toxic chemicals can contaminate water, air, and soil.

    How is firefighting foam contaminating the water?

    After AFFF is extinguished, the groundwater absorbs it. Once that happens, the carcinogens found in AFFF contaminate the water. When those living in the surrounding area drink the water, they ingest these toxins, which could be detrimental to their health.

    The government is aware of the health risk AFFF has imposed on the people who work with the product and who live in the vicinity of where it is used. According to the Governmental Accountability Office (GOA), the Department of Defense has taken action to prevent further harm. They have:

    • Installed water filtering systems
    • Provided more bottled water to residents

    They are continuing to investigate alternative ways to ensure that the water is free of PFAS.

    Does AFFF cause cancer?

    Because AFFF has carcinogens, it can cause cancer in both humans and animals. People who have been exposed to AFFF can suffer:

    • Breast cancer
    • Pancreatic cancer
    • Hodgkin’s lymphoma
    • Kidney cancer
    • Liver cancer
    • Prostate cancer
    • Testicular cancer
    • Ovarian cancer
    • Bladder cancer
    • Thyroid cancer and disorders
    • Leukemia

    If you are suffering from another type of cancer or illness after AFFF exposure, you still may be able to file an AFFF lawsuit. A lawyer in our network can review your situation and help determine your options.

    AFFF exposure symptoms

    You might not have been aware that you were exposed to firefighter foam, and now you might be suffering from health complications as a result. 

    Cancer can be difficult to detect, especially in the early stages, but if you are aware of the symptoms, you can start treatment as soon as possible. The ACS notes that the following could be symptoms of cancer:

    • Fatigue, no matter how much rest you’re getting
    • Sudden weight gain or loss
    • Swollen lymph nodes
    • Lumps in the affected areas (particularly in breast and testicular cancer)
    • Unusual and random bruising or bleeding
    • Headaches
    • Persistent cough
    • Fevers
    • Night sweats
    • Problems with eating
    • Jaundice (when the skin or area around the eyes turns a yellowish color)
    • Blood in urine or changes in urination or bowel movement patterns
    • Problems with vision and/or hearing
    • Sores or bleeding in the mouth

    Note that these are the most common symptoms of cancer. If you notice that there is anything abnormal about your body and how it functions, never brush off these symptoms. Go see your healthcare provider. 

    Seeking medical attention can keep your condition from getting worse, and it may also show a connection between your cancer diagnosis and your exposure to AFFF. That way, the manufacturer’s insurance company will find it more difficult to dispute your claim.

    People at risk of AFFF exposure

    The following people can be at risk of exposure to AFFF:

    • Residents in an area where AFFF was used, as their drinking water or soil from their garden could have been contaminated
    • Airport workers if an aircraft catches fire and AFFF was the only resource they had at their disposal to extinguish the fire
    • Military personnel if they needed to use AFFF to extinguish fires during training
    • Firefighters who suffered exposure to AFFF
    • Chemical plant workers who used AFFF

    Despite wearing protective gear, those who used AFFF at work could still risk exposure, as the product can seep in through other materials.

    Side effects of AFFF exposure

    How long, how much, and how often you were exposed to AFFF play a role in the side effects you can experience. The EPA points out that in addition to cancer, some other ailments you can suffer include:

    • High cholesterol
    • Hypertension and preeclampsia stemming from pregnancy
    • Higher amount of liver enzymes
    • Weaker response to vaccinations
    • Delays in fetal and childhood development
    • Low weight at birth
    • Other birth defects
    • Infertility
    • Compromised immune system
    • Asthma

    Filing an AFFF contamination lawsuit

    If you or a loved one has suffered from a disease or another complication that you believe stems from AFFF exposure, you have a right to hold the negligent party accountable for your damages.

    Depending on where you live in the United States, you can bring an AFFF lawsuit against one of these companies:

    • 3M Company
    • Tyco Fire Products
    • Chemguard
    • Buckeye Fire Protection Company
    • National Foam, Inc

    These companies, in addition to the ones not mentioned here, knew about the risks that AFFF imposed on users and bystanders for decades. They had an obligation to warn city and state governments about these dangers and failed to do so. Had they taken action earlier, many more lives could have been saved. Don’t let them get away with causing your illness.

    How do AFFF suits work?

    How AFFF lawsuits work depends on what type of legal action you would like to take: personal injury, class-action, or multidistrict litigation (MDL).

    A personal injury lawsuit

    A personal injury case allows a single individual to take legal action. A lawyer within our network can build a case around:  

    • The illness they have developed
    • Their financial and non-financial damages
    • Their prognosis if there is one

    A class-action lawsuit

    A class-action lawsuit is when a group of individuals who have suffered from a similar situation file one collective lawsuit to pursue compensation. Further, only one person from the group will speak on everyone else’s behalf and might even represent them in a trial. If the court awards compensation, then everyone in the group receives a portion.

    In the case of a firefighting foam lawsuit, the class-action route could be beneficial because:

    • Your experience with the company’s negligence will be heard.
    • It can cut down on litigation costs.

    For example, if you have minor complications from the exposure to AFFF, then pursuing a personal injury case might not be worth it after all the fees are deducted—you could be left with only a couple hundred dollars.

    So, if you wish to submit a class-action lawsuit after you have been exposed to and suffered the consequences of AFFF, a lawyer can file your complaint with the court and request permission for prospective clients to join your case.

    Multidistrict litigation (MDL)

    The last option you have for filing a firefighter foam lawsuit is via multidistrict litigation (MDL). In this scenario, multiple federal cases from around the country are disputed in one court. Here’s how it works:

    • Pretrial proceedings
    • Discovery phase, otherwise known as the investigation
    • Settlement conferences
    • Bellwether trials, which test a jury’s response to the evidence
    • Settlement negotiations if bellwether trials go through

    The judge will then urge each party to come to a settlement. If this step is not successful, then the cases will be sent back to the original courts for dispute.

    This method can be beneficial for claimants, as there are more lawyers involved who can pool their resources together. Like class-action lawsuits, MDLs can be more cost-effective for claimants. 

    Have any AFFF foam lawsuits been filed?

    Per DrugWatch, an increasing amount of AFFF foam lawsuits has been filed, particularly by firefighters who have received a cancer diagnosis. Over 950 claims under MDL are pending in South Carolina’s federal court system.

    Individuals are not the only ones to have taken action and filed an AFFF lawsuit. As such, many states are suing manufacturers, including 3M Company.

    What compensation is available in an AFFF lawsuit?

    You might be entitled to different forms of compensation in an AFFF lawsuit. The following list is not exhaustive, but among the most common damages are:

    • Past and future medical expenses: Your illness might have required you to have surgery, chemotherapy or radiation, diagnostic and blood tests, medication, and assistive medical equipment.
    • Past lost wages: If you were too sick to work, you might have missed out on bonuses, hourly pay, tips, vacation time, and other benefits.
    • Lost future earning potential: If you were forced to take on a job that doesn’t pay as much or you cannot go back to your original job, then we can request the difference in pay.
    • Property damage: If your home sustained damage due to the toxic chemicals from the AFFF, you can claim damages for repair or replacement costs.
    • Pain and suffering: This damage might include any physical discomfort or pain that comes with your illnesses and treatment.
    • Wrongful death damages: If you lost your loved one to the illness caused by AFFF, you may be able to recoup their final medical expenses and funeral costs, as well as your losses of financial support and companionship.

    The types and amount of compensation you are able to receive will vary depending on the specifics of your case, like your occupation, age, marital status, financial status, and quality of life.

    How do I know if I have a case?

    To determine whether or not you have a case, you must first prove that you were exposed to AFFF—whether as a resident in an area in which AFFF was frequently used or as a worker who used it on the job.

    Once a lawyer from our network shows this link, they can help prove the manufacturing company’s negligence using the following four tenets:

    • Duty of care: The manufacturing company was to use materials that would not cause harm or warn you of the dangers of the product.
    • Breach of duty: The company used hazardous materials in AFFF (which in this case would be PFAS), sold the product to the public, and failed to warn them about the dangers once it was made available.
    • Causation: Over time, exposure to AFFF caused you to develop cancer or another related illness.
    • Damages: Your illness and/or treatment has led to your medical bills, missed work, and pain and suffering.

    You must prove all four of these elements to have a valid case. Otherwise, it will not be accepted. 

    Evidence that can help your case

    To help back up each of these claims, you must have different forms of evidence, some of which may be:

    • Your work history: This category of evidence can demonstrate how long you were out of work, how much pay you missed, and the type of profession you had (e.g., military, firefighter, airport worker, etc.).
    • Your residence: If you were exposed to AFFF at your residence, proof of residence will be paramount if AFFF was used in that particular area. 
    • Medical records: Your medical records document when you were first diagnosed with your illness, your treatment plan, doctors’ appointments, the medication(s) you took, and the type of symptoms you suffered. You will also want to include your doctor’s input about where the illness could have stemmed from.
    • Medical bills: These bills will be the foundation of your personal injury case, as they will illustrate the cost of your surgery, medications, any medical equipment you needed (e.g., crutches or wheelchair), cancer treatments, hospital rooms, tests, and follow-up visits with your doctor.
    • Other people’s testimonies: It may be beneficial for you to get the contact information of your coworkers who used AFFF alongside you at work or your neighbors if they suffered from contaminated water, soil, and air. They can talk about their experiences and how they affected their way of life.

    You are not limited to showing only these forms of evidence. The smallest detail can make a world of difference in your fight for compensation.

    AFFF lawsuit settlement amounts

    The amount of compensation your AFFF lawsuit may yield depends on your situation and how you were affected. According to Quartz, a handful of lawsuits related to PFAS have been settled throughout the United States. To name a few:

    • DuPont and Chemours settled a lawsuit over 3,500 Ohioans and West Virginians after their product polluted a manufacturing plant located in Parkersburg, West Virginia. The case closed at $671 million.
    • Residents in Colorado, Michigan, New York, and Pennsylvania filed a class action case after exposure to water contaminated with PFAS. The lawsuit was settled at $13 million.
    • 3M Company agreed to pay $850 million to Minnesota after drinking water that had PFOA infused, according to Chemical & Engineering News.

    Firefighter foam cash settlements

    In January 2021, Tyco Fire Products settled with the residents of Wisconsin at $2.5 million in cash payouts. These people suffered from cancer, among other health complications, after their water was contaminated with PFOS that originated from firefighter foam.

    The settlement covered about $15 million in property damage for homes and wells that were no longer useful.

    Can I afford a lawyer?

    Most personal injury law firms work for a contingency fee. What this payment arrangement entails is:

    • When you first call the firm, a member of the staff will provide you with a free consultation that comes with no obligation or financial risk.
    • If you decide to partner with the firm, there are no fees required up front or out of pocket.
    • The lawyer is not paid by the hour or in a lump sum.
    • The attorney’s fees come out of your final settlement or court award. It’s usually about 30 to 40 percent of the damages, as the American Bar Association (ABA) details.
    • If your lawyer cannot achieve a favorable financial outcome for you, they will walk away from the case without charging for their services.

    When a lawyer works on a contingency-fee basis, you can obtain legal representation without risking further financial loss. Contingency fees also create an incentive for the lawyer to win your case. 

    However, it is important to keep in mind that even though the attorneys finance your case until the end, other fees might be deducted from your potential settlement or court-awarded offer. For example, if they hired medical experts or other professionals to testify or you need to go to court, there may be separate fees involved. You can discuss the payment plan with the firm we connect you with.

    Choosing an AFFF lawsuit attorney

    Choosing the right AFFF Lawsuit attorney for any situation, especially an AFFF lawsuit, is crucial. After all, they are going to be going up against big corporations and advocating for you after you have suffered from an illness that has upended so many areas of your life.

    When looking for the right personal injury attorney, it is recommended that you have the following in mind:

    • Check their track record: Many personal injury law firms have testimonials from previous clients, as well as their best case turnouts on their websites. This information can be a great indicator of what it is like to work with them.
    • Read about their practice areas: Personal injury law covers a wide range of areas, and not everyone handles product liability and/or class-action lawsuits. We have a nationwide network of law firms, and we can help connect you with one that can handle your case.
    • Their overall experience in the legal world: While you’re doing research, ask yourself questions about what you’re looking for in legal representation. How long has this firm been practicing? What parts of the country do they work in or are they familiar with? Do they usually take lawsuits to trial if it comes to that? What are their recognitions or achievements?

    Whenever you read practice area pages on lawyers’ websites, they typically talk about the services they provide for their clients. They usually take on the following responsibilities:

    • Gathering, analyzing, and organizing evidence: Finding all forms of evidence on your own can be tedious and very daunting, so you should allow your lawyer to collect your medical records and bills, interview others who are in a similar situation to yours, take your account of what happened, and request access to your work records.
    • Identifying the liable party: We can look to see which manufacturer was responsible for providing the AFFF and ultimately contaminating your environment—whether it be at home or work.
    • Communicating with the parties involved: Talking to these big corporations’ insurance companies and legal teams on your own can be overwhelming. Your lawyer should have experience in this area, and they can communicate with the liable party and their representatives on your behalf. 
    • Maintaining consistent communication with you: If you are ever unsure about the legal process in general or your AFFF lawsuit, you shouldn’t hesitate to reach out to your assigned lawyer. They should be providing you with frequent case updates anyway.
    • Adhering to your state’s statute of limitations: Unfortunately, you don’t have forever to file your firefighting foam lawsuit. All states imposed a deadline in which you have to bring your lawsuit against the liable party. Your lawyer should be able to identify which one applies to your case and then help you comply with it.
    • Negotiating a settlement with the insurance company: Your AFFF lawsuit lawyer should be able to determine a low settlement offer from a sufficient one. If the insurer offers you the former option, your lawyer is to negotiate with them until both sides can agree on an amount. If that is not possible, then going to court might be the next step for your case.
    • Taking your AFFF lawsuit to trial: Not all personal injury law firms are willing to go to court and prefer to settle beforehand. Since your situation involves big companies, there is always that chance that it could go to trial. While you research, make sure you ask about the firm’s experience in the courtroom.

    This list is just a general sense of what the lawyers should be able to do for you when they take on your firefighting foam lawsuit.

    Get in touch with the Sentinel Group for your AFFF lawsuit today

    The Sentinel Group is a referral service that helps you find the right law firm when you are looking to file a firefighting foam lawsuit. Don’t settle for dealing with the repercussions of contaminated water, soil, and air at work or home. We can connect you with mass tort lawyers who can help you hold the manufacturers responsible for their negligence.

    Fill out our contact form today for assistance with your case.

  • Philips CPAP Lawsuit | Sleep Apnea CPAP and BiPAP Machine Lawsuit

    Philips CPAP Lawsuit | Sleep Apnea CPAP and BiPAP Machine Lawsuit

    Philips CPAP Lawsuit

    A Simple Guide to CPAP Lawsuits and Settlements

    Philips, a medical device manufacturer based in the Netherlands, initiated a voluntary recall notification in June 2021 for several bi-level positive airway pressure (BiPAP), continuous positive airway pressure (CPAP), and mechanical ventilator devices the company produces. The recall affects people in both the United States and Europe who use these products to treat their sleep apnea.

    These recalled breathing devices contain polyester-based polyurethane (PE-PUR) sound abatement foam, which degrades into small particles that have carcinogenic effects if inhaled or ingested. If you or a loved one developed serious health problems after using one of Philips’ recalled CPAP machines, you may qualify to file a Philips CPAP lawsuit against the manufacturer and pursue compensation for your injuries.

    Check this list to see whether Philips recalled your CPAP or BiPAP machine product

    Philips sent out a recall on several medical devices used to treat obstructive sleep apnea. Each breathing device mentioned uses PE-PUR foam and other volatile organic compounds (VOCs) that can lead to cancer and other serious health conditions if inhaled.

    Patients who own and use any of the recalled items should stop use immediately and consult their physician for further instruction on treatment and potential health problems.

    Recalled CPAP and BiPAP devices

    If you used one or more of the following CPAP, BiPAP, or ventilator devices, you may have grounds to file a defective product lawsuit against Philips:

    • DreamStation ASV
    • DreamStation GO CPAP, APAP
    • DreamStation CPAP, Auto CPAP, BiPAP
    • DreamStation ST, AVAPS
    • Dorma 400 CPAP
    • Dorma 500 CPAP
    • REMStar SE Auto CPAP
    • C Series ASV
    • C Series S/T and AVAPS
    • SystemOne ASV4
    • SystemOne (Q-Series)
    • E30 (Emergency Use Authorization)
    • OmniLab Advanced Plus (In-Lab Titration Device)

    This list includes all devices manufactured before April 26, 2021, based on when Philips sent out a company report on its first quarter results.

    Continuous ventilators that may be used as alternatives

    Philips did not recall every CPAP, BiPAP, and ventilator device they have out in the market, so there are alternatives that patients can use to treat their sleep apnea, such as:

    • Trilogy 100 Ventilator
    • Trilogy 200 Ventilator
    • BiPAP V30 Auto Ventilator (A-Series)

    Philips listed other alternative continuous ventilator devices; however, these devices are not marketed in the United States.

    Other Philips products do not use the same sound abatement materials or technologies as the recalled items, so patients can continue to use these products. These items include:

    • Trilogy Evo, Evo OBM, EV300, and 202
    • DreamStation 2 Auto CPAP Advanced and DreamStation 2 Auto CPAP
    • OmniLab and OmniLan Advanced Titration devices
    • REMStar SE and Sleep Easy CPAPs
    • V60, V60 Plus, and V680 Ventilators
    • A-Series Pro and EFL
    • Respironics M-Series REMStar CPAPs, Auto CPAPs, and BiPAPs

    If you are unsure what make and model your product is, you can consult your physician to review which products you are using for treatment.

    PE-PUR foam degradation can cause side effects, including cancer

    In response to Philips’ CPAP machine recall, the U.S. Food and Drug Administration (FDA) also sent out a notice to people in the United States about the recall and provided more information about the health risks attached to the medical devices. The FDA also initiated inspections on Philips Respironics’ manufacturing facilities to limit as much potential for product defects as possible. 

    According to the FDA, the ventilator, Bi-PAP, and CPAP machines recalled may cause side effects such as:

    • Cancer
    • Organ damage, such as to the kidneys or liver
    • Inflammation
    • Irritation in the respiratory tract, eyes, and skin
    • Asthma and other breathing difficulties
    • Nausea and vomiting
    • Headaches and dizziness
    • Hypersensitivity

    If you are experiencing any of these symptoms, consult your physician and inform them about the breathing device you use, as it may be related to your health. At the time of the FDA’s notice (June 2021), there were already more than 1200 filed complaints about Philips’ Respironics products and 100 filed injury reports.

    A CPAP attorney can help you build a case against Philips

    After Philips recalled millions of its sleep apnea medical devices, law firms across the United States are now searching for affected individuals who might qualify to file a class action lawsuit against the manufacturer. 

    Whether you or a loved one has already developed negative side effects due to long-term use of one or more of Philips’ products or you could be at risk of serious health consequences later on, a lawyer near you can represent your case and help you hold the manufacturer liable. 

    A lawyer can calculate the value of your case by assessing your damages

    With a defective product case, you can pursue compensation for your injuries and related damages from Philips. Your personal injury lawyer will review your damages and categorize them based on whether they have a financial value (economic damages) or must be assigned one (non-economic damages). This aspect of building your case is crucial, as it determines how much compensation you should pursue based on your current and potential losses.

    In short, economic damages include all financial losses you suffered because of your injuries. For example, if you developed lung cancer as a result of using one of the recalled DreamStation CPAP machines, then you may qualify to pursue compensation for:

    • Medical care costs, like costs for chemotherapy, prescription medicines, diagnostic exams, emergency room treatment, hospitalization, and surgeries
    • Medical equipment costs, such as costs to replace your CPAP machine and other support devices since developing cancer, like oxygen tanks
    • Income loss related to missing work to get treatment for your injuries or because of limitations that prevent you from working
    • Future income loss if your injuries are long-term or permanent (e.g., permanent organ damage that rendered you disabled)

    Non-economic damages encompass physical and emotional injuries, which are subjective. Law firms vary their approach to measuring these damages, but your legal team can explain their process for evaluating your non-economic damages. The goal is to reach a value that reflects the overall impact of the plaintiff’s injuries on their life, which can include:

    • Pain and Suffering, both physical and emotional pain
    • Permanent disability, such as permanent respiratory problems
    • Loss of enjoyment in hobbies and activities, such as sports and regular exercise
    • Diminished quality of life
    • Emotional distress, which includes depression and anxiety
    • Physical disfigurement, which includes scarring from surgical procedures

    Our examples are not the only forms of compensable damages, so your personal injury attorney may suggest other damages to include in your demand letter for compensation.

    Law firms often provide other services to help clients build their cases

    If you have never filed a personal injury case, you don’t have to attempt to navigate the claims or litigation process on your own. A lawyer who handles product liability cases can manage your Philips CPAP lawsuit for you and lead their team to collect information that supports your case against the manufacturer.

    Many law firms offer to:

    • Investigate your case: If you suspect your sleep apnea device released PE-PUR foam particles into the open air paths of the device and caused you to develop side effects, our team can review the device’s serial number to see if it qualifies with the recall. We may also consult your medical records or care providers with your permission to see if there is a connection.
    • Collect evidence that supports your claims: Once we establish a correlation that holds Philips liable for your injuries, we will help you gather evidence. This evidence can include your medical records, product test results, video footage, and expert witness analysis, among other documentation.
    • File paperwork on your behalf: Litigation often involves extensive paperwork that can be confusing and difficult to comprehend for those unfamiliar with legal jargon or procedures. Your lawyer can interpret and fill out the required forms for your case and submit them by their deadlines for you, including the Philips CPAP lawsuit with your state’s court system.
    • Communicate with involved parties on your behalf: Once you send a letter of notice about your intention to sue, the manufacturer’s legal team may reach out to you for a statement or to settle your case. Handling these communications yourself might put you at risk of admitting partial fault or undervaluing your case. Instead, you can refer any inquiring parties to your CPAP lawsuit attorney for response and protect your case in the process.
    • Negotiate a potential settlement: Whether you file an insurance claim or product liability lawsuit, your injury attorney may make efforts to avoid going to court altogether and reach out to the other party to negotiate a settlement. They can attend meetings on your behalf to advocate for your interests and then inform you about any settlement offers you receive. You have the final word, so you decide whether to accept a deal or continue negotiating.
    • Represent you in trial: If you decide to pursue a case in court, your personal injury lawyer will serve as your legal representative and present you in trial to a judge and jury. Here, you will get a verdict, which determines whether you receive compensation or not for your injuries.

    As a client, you can refer to your lawyer to ask questions or express concerns about your case and you will receive guidance on what the legal process entails, options you have to move forward, and realistic projections for your case.

    You will receive guidance from your lawyer as you navigate the litigation process

    Personal injury lawyers navigate all sorts of cases and build strategies based on the cases they’ve handled. Regarding your Philips medical device lawsuit, you may refer to your CPAP lawsuit lawyer for guidance involving:

    • Whether you should file an individual lawsuit or join a mass tort: Mass torts involve similar but individual cases against one defendant, usually with plaintiffs being from the same geographic area. Their claims typically go through multidistrict litigation (MDL) as a way to consolidate actions filed against one defendant. Your lawyer can describe the pros and cons of joining a mass tort and also explain options to file individually.
    • Whether you should file a personal injury lawsuit or insurance claim: Some plaintiffs opt to file an insurance claim to avoid going to trial. Your lawyer can explain whether you qualify to file a personal injury lawsuit instead and whether it might be in your interest to do so.
    • What’s considered a “fair” settlement offer: You do not want to risk undervaluing your case, so while thousands of dollars might sound appealing now, it might not be enough if your injuries put you through a lifetime of medical costs that exceed the offer you receive. Your lawyer can calculate your approximate damages and use this figure to measure when you should consider an offer or keep negotiating for more compensation.

    Each defective product case brings its own unique circumstances, so you may have personal questions, which your lawyer can address after becoming familiar with your case.

    Your time is limited if you want to file a personal injury lawsuit against Philips

    Many states set a statute of limitations on personal injury cases, which limits the timeframe plaintiffs have to file lawsuits against defendants. If you would like to file a lawsuit against Philips about an injury caused by one of its products, consult your attorney about your case’s filing deadline.

    You do not want to miss your case’s filing deadline as it could jeopardize your ability to pursue compensation. Once a judge dismisses a case, whether upon reviewing it or after the defendant requests a dismissal, you will be barred from pursuing compensation through the court system and then lose any legal leverage against Philips.

    This outcome can limit your ability to keep negotiating a settlement, as you won’t have the threat of a lawsuit on your side.

    How does a CPAP machine work?

    Because sleep apnea is a health condition that involves breathing obstruction during sleep, the prime objective of CPAP and related machines is to prevent users from experiencing airway blockages so that they can sleep fully throughout the night.

    CPAP machines produce a steady flow of oxygen through their pumping systems and blow purified air through tubing into the user’s nose and/or mouth. The user generally must wear a mask to attach the tubing to their nose and/or mouth, though masks vary by machine type.

    What is the difference between CPAP and BiPAP machines?

    The differences between CPAP and BiPAP machines include:

    • Continuous positive airway pressure (CPAP) machines: These machines send out purified air at one air pressure level so that it remains steady throughout the evening. Users must manually reset settings if they want to change the air pressure level.
    • Bi-level positive airflow pressure (BiPAP) machines: People who cannot sleep well with CPAP machines may use BiPAP machines instead, which exchanges between two different air pressure levels for inhalation and exhalation. BiPAP machines can also report backup respiratory rates for people who suffer from central sleep apnea, which can help people breathe better, per Healthline.

    With the Philips-brand CPAP, BiPAP, and ventilator machines, the issue is not in how the machines produce air for users but in the materials surrounding the mechanisms. If your sleep apnea machine is experiencing mechanical dysfunctions that prevent it from working properly at night, you may qualify for a separate defective product lawsuit concerning those errors. If so, a lawyer may review your case and explain your legal options.

    Why are the Philips CPAP machines considered unsafe for sleep apnea patients?

    Philips’ recall applies to its CPAP, BiPAP, and ventilator machines that use polyester-based polyurethane (PE-PUR), which is a sound abatement foam. This foam helps reduce noise made by the sleep apnea machines, which allows users to sleep better and with less disturbance from vibration.

    However, the issues with the PE-PUR foam used in the recalled products is that:

    • PE-PUR breaks down into small particles over time.
    • These particles can slip into the medical devices’ air passageways, such as through the tubing or the air pump system.
    • Users can inhale or ingest the particles while sleeping and thus without realizing. 
    • These particles contain chemicals that have carcinogenic effects when introduced to the body. The particles can also cause irritation and damage throughout users’ respiratory tracts, which include the nose, throat, and lungs.

    The FDA also noted in its recall that “foam degradation may be exacerbated by high heat and high humidity environments, and by use of unapproved cleaning methods, such as ozone.” So, for example, if a person lives in a state that has high levels of humidity (e.g., Florida) or heat (e.g., Arizona), their sleep apnea device may have started the PE-PUR foam degradation process and should be inspected.

    What is the single biggest challenge victims face in their CPAP lawsuits?

    Plaintiffs who file product liability lawsuits against Philips will need to establish a direct correlation between Philips’ recalled products and their injuries. Your legal team may conduct an analysis and help you build a case argument that centers on Philips’ negligence as a medical device manufacturer, but how a plaintiff might argue negligence depends on the approach they take with their case.

    You must establish how Philips holds liability for your injuries

    Some plaintiffs might use a strict liability structure to shape their case argument, meaning their case focuses on the fact that the plaintiff bought a defective product and the manufacturer is liable for products it sells in the public market.

    This argument involves establishing these key points:

    • You purchased the Philips CPAP/BiPAP/ventilator machine: Whether you purchased the item through your health insurance or out of pocket, you must establish that a transaction occurred. You can also provide your medical records to establish why you bought the item (e.g., to treat your sleep apnea).
    • You did not know the product had defects before the Philips medical device recall: For this point, your lawyer may help retrieve medical information about the sleep apnea product you used that was available before the recall. They might also retrieve testimony from the medical care provider that prescribed the device to you to confirm what information was available at the time you began using the product.
    • The product contains a defect that puts your health at risk: Next, you must prove the product is defective, so your legal team can work to get a consumer expectations test done. Per the Legal Information Institute (LII), this test allows juries to determine whether a product failed to perform to its expectations and then judge the risk level it forces on consumers.
    • The product led to your injuries: Finally, you must establish the correlation between the product’s defects and your injuries. For example, your lawyer may argue that you inhaled PE-PUR foam particles through the tubing while sleeping for years, so you then developed respiratory problems after the particles scratched and irritated the lining of your nose, esophagus, and lungs.

    While each case against Philips may be unique, plaintiffs can join a mass tort against the manufacturer to hold it liable for negligence. With mass torts, plaintiffs can leave litigation matters in the hands of their attorneys, which can be beneficial when taking on big corporations. By having multiple claims filed against one defendant, the collective can support each other in their arguments and establish more credibility.

    If plaintiffs argue Philips knew of its product defects before the recall

    Another legal strategy against Philips involves arguing whether the company knew about the product defects long before the recall in June. Some law firms assert this is possible due to the manufacturer’s recent DreamStation product launch in April 2021, which is said to be a safer alternative and does not experience the same issues with PE-PUR foam degradation.

    The company would later issue a recall in June 2021, several weeks after launching a safer alternative. Your attorney may look into efforts the manufacturer might have made to cover up defect information about their products before the recall, which they might find through other complaints made against Philips.

    Surviving families of victims who lost their lives to Philips products can sue

    Because some Philips CPAP lawsuits involve victims who developed cancer after PE-PUR foam exposure, unfortunately, there may be cases where the victim cannot speak for themselves. If you lost a loved one to cancer or another fatal health condition caused by their CPAP/BiPAP/ventilator machine, you may qualify to file a wrongful death action, which would allow you to pursue compensation on their behalf. 

    A wrongful death lawyer near you can represent your case and advise you throughout the legal process. 

    Can any family member file a wrongful death action against Philips?

    This answer varies by state. In most states, eligible family members are limited to the decedent’s (passed individual):

    • Surviving spouse
    • Surviving child
    • Surviving parent
    • Personal representative

    However, other states may allow surviving grandparents, siblings, aunts or uncles to file a wrongful death action if no other surviving family member exists. Your attorney can explain the qualifications you must meet to file a wrongful death claim or lawsuit in your state, then take appropriate measures to submit your case to the court system.

    What kind of damages can you pursue in a wrongful death case?

    When a family member files on behalf of their deceased loved one, they can pursue damages that relate to their death as well as the damages that the victim would have pursued themselves had they remained alive. For example, common wrongful death damages include:

    • Costs for funeral arrangements
    • Costs for burial or cremation services
    • Medical debts related to the treatment the decedent received up until their death (e.g., costs for chemotherapy, surgeries, and hospitalization)
    • Loss of financial support from the decedent if they contributed to the family net worth but were unable to because of their illness
    • Future loss of financial support now that the family must survive without their loved one
    • Loss of consortium and other significant changes to relationship dynamics
    • Loss of parental guidance, love, and affection
    • Loss of inheritance
    • Pain and suffering experienced by both the decedent and the surviving family

    Depending on your state’s statute of limitations for wrongful death actions, your time restraints may conflict with your mourning period. Many lawyers understand the difficulties in trying to balance grief with legal matters, which is why many firms take on the legal responsibility to manage their clients’ cases right away so that they do not have to worry about missing their legal deadlines.

    Throughout the case-building process, your lawyer may suggest other damages unique to your family’s circumstances, and they will update you as your case progresses through litigation.

    Fill out our contact form to get help with your Philips CPAP lawsuit

    If using one of Philips’ BiPAP or CPAP machines caused you to suffer negative side effects and develop an illness or serious health condition, you may be entitled to file an individual personal injury lawsuit or join a mass tort action.

    Fill out our contact form to get connected with a personal injury lawyer and start your legal journey today. A mass torts lawyer serving your area can help you build a case against Philips and pursue compensation from the company.

    Related Links

    Philips CPAP Lawsuits: Device Replacement Problems Leave Recall Issues Unresolved
    FDA Calls on Philips to Repair or Replace Defective Ventilators
    Phillips CPAP Recall Breaking News Update
    Join A Class Action Lawsuit Against Philips CPAP Machine

  • Are Hernia Mesh Lawsuits Real?

    Are Hernia Mesh Lawsuits Real?

    Yes, hernia mesh lawsuits are real. Many people in the United States have had health complications as a result of defective hernia mesh products and have filed lawsuits against mesh manufacturers. You could also be eligible for damages if you had side effects due to an implant. A hernia mesh lawyer can help.  

    What are the symptoms of hernia mesh failure?

    Hernia mesh failure has a number of symptoms that can range based on: 

    • The type of hernia mesh
    • The form of hernia mesh repair surgery entailed
    • The hernia site

    According to the U.S. Food and Drug Administration (FDA), your symptoms can vary depending on whether or not you have a recalled mesh product. More recent hernia mesh implants come with side effects such as:

    • Pain: Pain following hernia mesh surgery can become chronic. 
    • Infection: Signs that hernia mesh sites have become infected include fever, flu-like symptoms, or inflammation.
    • Hernia recurrence: This is when another hernia forms even after you receive a hernia mesh implant.
    • Adhesion: This refers to a kind of scarring that causes other organs or tissue to improperly bind to the mesh. 
    • Bowel obstruction: Bowel obstruction could also result from unintended mesh adhesion. Per Mayo Clinic, intestinal obstruction could entail constipation, abdominal swelling, issues with appetite, and problems with bowel movements.
    • Mesh migration: This occurs when the mesh shifts to another site in the body. If the mesh migrated, you may experience fever, nausea, vomiting, unusually warm skin close to the surgery site, fluid build-up beneath the skin, or pain.
    • Mesh shrinkage: When hernia mesh shrinks, local tissues can be stretched or damaged, leading to pain.

    These symptoms, along with others, are also common with older mesh products (mesh not currently on the market). Additional symptoms with older implants include tissue perforation and bowel perforation.

    One study from the Journal of the American Medical Association (JAMA) notes that some forms of hernia mesh repair can lead to complications in nearly 6% of patients. This study observed hernia mesh complications and follow-up procedures over a five-year period, demonstrating that hernia mesh repair can entail long-term complications. 

    Additionally, certain forms of hernia surgeries come with their own risk of complications. As Healthline notes, inguinal hernia repair (hernia surgery at the groin) may involve risks to blood vessels in the area, such the testes. You could also face nerve damage or other organ damage in the treated areas.

    What are the potential damages for hernia mesh injuries?

    In a hernia mesh lawsuit, you could seek a number of compensatory damages, depending on how the injury affected you. Both financial and non-financial damages could be available. 

    Economic damages (your monetary losses) 

    These are damages that caused you financial losses as a result of your hernia mesh implant, which may include:

    • Medical bills, such as for revision surgery, surgery to remove a defective mesh, care related to hernia recurrence, emergency care, diagnostic testing, surgery, physical therapy, visits to a doctor, medications, and more
    • Lost wages, including income you missed due to the time spent recovering from injury
    • Reduced earning capacity if you will be unable to earn the same income as you did before your injury
    • Other out-of-pocket costs, such as for medical assistive devices, like home modifications

    Keep in mind that these damages can account for your past, present, and future losses. So, if you anticipate the need for additional hernia repair surgery, you can seek an award for that expense, as well. 

    Non-economic damages (your non-monetary losses) 

    These are losses that have no clear dollar value but have caused losses nonetheless. They include:

    • Pain and suffering for your physical pain and other related challenges
    • Mental anguish for psychological harm
    • Loss of consortium if the injury prevents you from being intimate with your spouse
    • Loss of enjoyment of life if you have lost interest in hobbies and activities you enjoyed before the injury

    Hernia mesh lawsuits have not yet been settled, and there is no predetermined amount that a claimant can expect. Your damages may be awarded based on unique factors, such as your medical bills and how severely your injuries have affected your work and life.

    You may seek legal help because calculating and proving your damages—especially your non-economic losses—can be complicated. For example, let’s say that your hernia mesh implant caused  severe abdominal pain that left you unable to work. As a result, you may have experienced lost wages, as well as depression due to your shift in employment status. 

    In this situation, if you can show compelling evidence of your medical prognosis, your mental health condition, and your need to take on a new line of work due to your health complications, you may have a good case for fair compensation. If you don’t show strong evidence of these damages, your case may not yield the awards you expect.

    How do I know if I qualify for a hernia mesh lawsuit?

    Your symptoms could be related to your hernia mesh implant. If so, we can help you determine if you have a case. 

    A law firm we connect you with will consider such details as:

    • The complications you’ve had since your hernia mesh implant 
    • Your medical prognosis 
    • When you had your surgery
    • Which hernia mesh product was involved

    A legal team in our network can tell you more about whether or not you can pursue a hernia mesh lawsuit.

    Filing a hernia mesh lawsuit based on negligence or product liability

    Depending on the details of your case, we may have grounds to file a lawsuit based on product liability or medical negligence. A hernia mesh attorney can pursue a case in either of two legal scenarios:

    • If a doctor or other medical provider’s failure to provide proper care caused your injury
    • If a hernia mesh maker’s design, manufacturing, or improper labeling was responsible for your injury

    Read on below to learn more about what it takes to prove medical negligence or product liability. 

    Hernia mesh lawsuits based on defective design

    If the materials or other aspects of the hernia mesh’s design were the cause of your injury, you may have a defective design case against the product manufacturer. The hernia mesh manufacturer does not need to have known of the defective design to be liable for a defective product.

    One case of defective hernia mesh design involved the Kugel Patch created by Davol, Inc. The FDA issued recalls of several Kugel Patch products in 2006 after reports of product failures, and Davol, Inc. is no longer marketing the product in the United States. 

    The design defect was related to the raised ring that allowed the patch to hold its shape. After surgery, the ring could become distorted, breaking or bending in the body. This defect led to complications such as:

    • Mesh migration
    • Bowel obstructions
    • Punctures
    • Fistulas

    In one settlement related to the Kugel Patch, Davol, Inc. paid over 2,600 plaintiffs $184 million in damages. 

    Hernia mesh lawsuits based on manufacturing defects

    In a product liability case, the design of the product may be safe and adequate for patient use, but the way the hernia mesh was manufactured led to defects.

    With Bard Davol’s Kugel Patch, this product was found to contain both design defects and manufacturing defects. The Kugel Patch was made of poor-quality polypropylene. While polypropylene is a standard material used in hernia mesh manufacturing, the Kugel Patch products were made of an unsafe form of this material. 

    A manufacturing defect could result from:

    • Choices to cut costs and use substandard, non-medical grade materials
    • Assembly errors
    • And more

    Hernia mesh lawsuits based on failure to warn

    A medical product or procedure may come with risks, and medical product manufacturers are expected to disclose those risks. A hernia mesh maker must also label a product so that medical providers are aware of any risks involved with the product and how they can manage those risks.

    In these kinds of cases, plaintiffs and their legal teams may be able to show that a hernia mesh product did not contain adequate labeling for this purpose. 

    Medical malpractice and hernia mesh lawsuits

    If your medical provider improperly implanted your hernia mesh, you may not have a product liability case. Instead, this could be a case of medical malpractice.

    These kinds of cases need to prove that a medical provider—either a doctor, nurse, or another provider—deviated from the normal standard of care they owed all patients. Four elements of medical malpractice must be established through compelling evidence:

    • The provider had a duty of care: This is relatively straightforward to prove if you were a patient, as doctors and other medical staff have a duty to care for a patient.
    • They failed to uphold their duty of care: Here is where the case will require more substantial evidence. You will need to prove that the provider was careless, reckless, inattentive, or otherwise negligent in their duties to provide a normal level of care.
    • Their failure led directly to your injury, also known as causation: It will need to be clear that the provider’s negligence was the reason you were injured. In other words, your hernia mesh surgery complications were not the result of a defective product or your own pre-existing health conditions. This element also requires substantial evidence, such as medical expert testimony.
    • You suffered damages as a result: Damages can take the form of financial and non-financial losses, such as the cost of additional mesh repair surgery or lost wages.

    Medical malpractice cases are especially complicated, and you may not want to deal with your case on your own while you are recovering. To prove your case, you may need expert testimony to speak to these medical details, including:

    • Defining what reasonable care would look like in your case
    • Pinpointing the actions or inactions that deviated from that standard
    • Demonstrating that those actions or inactions caused your past or current health outcome

    A lawyer who handles medical malpractice cases will typically have medical industry contacts who may be able to speak to these issues in your case. Again, the importance of building compelling evidence is key if your hernia mesh case resulted from a provider’s negligence.

    Who is the defendant in a hernia mesh lawsuit?

    Whoever was responsible for the design, manufacturing, and labeling of your product could be liable for your damages. In a hernia mesh lawsuit case, the defendant could be one of many possible hernia mesh manufacturers. 

    Atrium – Maquet – Getinge Group: C-QUR

    The hernia mesh product known as C-QUR may contain manufacturing and design defects. The product’s coating is made from fish oil, which can lead to side effects, such as adhesion and infection. Atrium Medical would be the defendant in a lawsuit involving this product.

    Covidien – Medtronic: Parietex

    Covidien LLC, a subsidiary of Medtronic, issued recalls of its hernia mesh product known as Parietex Composite Parastomal Mesh. These meshes caused recurring hernias, pain, and other side effects.

    Davol – C.R. Bard: ST hernia patch products

    Davol, Inc. (a subsidiary of C.R. Bard) may face hernia mesh lawsuits involving several of its products, including its ST hernia patches.   

    Davol – C.R. Bard: Composix Kugel patch

    These Kugel patches contained a defective ring design that caused the product to bend or break, leading to their migration. Again, Davol, Inc. may be liable due to these defects.

    C.R. Bard: 3DMax

    Designed for inguinal hernia repairs, these 3DMax meshes are especially lightweight and made with an anatomical shape. After surgery, these meshes can deteriorate, migrate, or cause other complications over time.

    C.R. Bard: PerFix Plug and Marlex

    This polypropylene plastic was trademarked by C.R. Bard and used to produce a number of hernia meshes, such as the company’s PerFix Plug. However, this plastic can degrade over time.

    Ethicon – Johnson & Johnson: Proceed Mesh

    Ethicon, Inc., a subsidiary of Johnson & Johnson, could be liable for mesh defects related to the product called Proceed Mesh. Ethicon, Inc. recalled thousands of its own Proceed mesh units because they eroded in the body. 

    Ethicon: Physiomesh

    The Physiomesh was another mesh product made by Ethicon, Inc. that led to complications after surgery, including hernia recurrence. The company issued recalls with this product, as well.

    Ethicon: Prolene Hernia System (PHS)

    Often used for inguinal hernia repair, the defects found in these hernia meshes have led to lawsuits due to health complications, such as chronic pain.

    What is the average payout for a hernia mesh lawsuit?

    There is no average payout for a hernia mesh lawsuit, as these suits vary based on:

    • The hernia mesh product involved
    • The extent of the damages caused by the product
    • The negotiated settlement or court award in each case
    • And other factors

    However, you could be able to seek damages that would cover the extent of your losses, including both financial and non-financial losses. 

    Payouts for plaintiffs in multidistrict litigation cases

    If you are joining a hernia mesh lawsuit as a plaintiff in a multidistrict litigation (MDL) case, you will become part of a larger group of plaintiffs across the country who have been similarly injured. Some current hernia mesh lawsuits are already in litigation as MDLs. 

    There are some advantages involved in seeking damages through an MDL case. These include:

    • You can still seek damages even if your injuries are relatively minor. 
    • You can combine legal resources with others to seek justice and compensation.

    Depending on how an MDL proceeds, the liable manufacturers may work out a settlement with the entire class of plaintiffs, or they may settle with individual law firms representing the plaintiffs.

    How much compensation have some plaintiffs already received?

    Some cases against hernia mesh manufacturers are already settled or received verdicts. This includes the $184 million settlement from C.R. Bard/Davol, Inc. in 2011. This is the largest hernia mesh settlement to date. 

    Many hernia mesh settlements are still in litigation, such as the Physiomesh lawsuits against Ethicon, Inc., as well as suits against C.R. Bard/Davol, Inc. and Atrium Medical. There are many lawsuits pending against these companies across the country, and more are in process with the state courts. 

    In many of these cases, trial dates are scheduled for 2021. The settlement amounts for these lawsuits have yet to be determined.  

    Is the hernia mesh litigation a class-action lawsuit or individual lawsuit?

    Hernia mesh lawsuits take the form of individual lawsuits, and then many may be consolidated into multidistrict litigation (MDL) cases. These multidistrict litigation cases allow multiple plaintiffs—in some cases, thousands of plaintiffs—to bring a case against one defendant for similar damages. 

    Multidistrict litigation (MDL) cases differ from class-action lawsuits, however.  

    For instance: 

    • An MDL against Atrium Medical is currently in litigation, as of September 29, 2021. With thousands of lawsuits filed against the manufacturer for defects related to C-QUR mesh, litigation has been stalled due to the Coronavirus pandemic. 
    • An MDL against Ethicon, Inc. is in litigation, as of September 29, 2021. Thousands of cases have been brought for the company’s Physiomesh Composite product. Like the MDL against Atrium Medical, these trials were also postponed during 2020.
    • An MDL against C.R. Bard/Davol Inc. also has thousands of cases filed for its polypropylene mesh products. This MDL is still in litigation, as of September 29, 2021. 

    How big will a hernia mesh settlement be?

    There is no way to estimate how much a potential hernia mesh settlement may be. As many of these lawsuits are still in litigation, the settlement amounts are unclear.

    However, you should know that the settlement amounts may be influenced by the outcome of the initial bellwether trials in each case. A bellwether trial is for an individual case involved in the MDL used to determine representative damages for the suit, among other purposes. If the bellwether trials have a positive outcome, this could push the defendants to pursue a settlement. 

    The law firms representing plaintiffs in these cases will work to seek a fair settlement. In the 2011 case against C.R. Bard/Davol, Inc., $184 million was divided among plaintiffs. 

    When will hernia mesh settlements happen?

    Trial dates for the MDLs against hernia mesh manufacturers have been postponed due to the Coronavirus pandemic, and many of these cases were scheduled to resume in mid-2021. 

    If you file a lawsuit for a hernia mesh case and you hire a law firm, an injury lawyer can update you about the progress of your case. If they receive news of any settlement offers, you will be informed. 

    Get help from hernia mesh lawsuit lawyers

    You don’t have to face the complications of a hernia mesh lawsuit on your own. We can refer you to a law firm within our nationwide network. Fill out our contact form for help with your case today.

    Related Links

    What is the Status of the Hernia Mesh Lawsuits?
    Can I Sue for Hernia Mesh?
    What is the Average Payout for Hernia Mesh Lawsuits?
    Whats Going on With the Hernia Mesh Lawsuits?
    How Far in Litigation is The Hernia Mesh Lawsuit?

  • Mesothelioma Lung Cancer Lawsuit

    Mesothelioma Lung Cancer Lawsuit

    Can I Sue for Asbestos Exposure?

    You can sue the company that manufactured the asbestos product for their negligence in exposing you to dangerous levels of asbestos. In some cases, you might be able to pursue your employer for workers’ compensation benefits. By pursuing damages from the at-fault party, you could receive compensation for your medical expenses, income loss, and pain and suffering.

    An asbestos lawsuit attorney can show you how to prove the connection between your work environment and your recent health care diagnosis. While pursuing a financial settlement, they can also represent family members of men and women who worked in asbestos environments and suffered due to second-hand exposure.

    Dangers and risks of asbestos exposure

    According to American Cancer Society (ACS) research, we have known about the dangers of asbestos as early as the 1900s. Asbestos damages the lungs and can create cancer cells when its particles are either inhaled or swallowed by people who handle products that contain it.

    If asbestos exposure harmed you, it may also take a toll on your family and on your finances. The Centers for Disease Control and Prevention (CDC) describes the danger of exposure to asbestos. Its research cites the following adverse health conditions that are the result of such exposure:

    • Asbestosis: A scarring of the lungs that leads to difficulty breathing
    • Pleural disease: A thickening of the membranes around the lungs and chest cavity 
    • Lung cancer: A cancerous tumor that invade the lungs and make breathing difficult
    • Mesothelioma: A rare cancer that surrounds the lungs, chest cavity, and abdominal cavity 
    • Other forms of cancer: Including larynx, ovarian, pharynx, stomach, and colorectal

    Being exposed to asbestos and its dangers often affects people who work in demolition, construction, home maintenance, home repair, shipyard, and property remodeling. If you or someone you love was injured in these or any other industry where you came into contact with asbestos-containing products or their airborne asbestos fibers, you may have the basis of a civil lawsuit.

    Filing a mesothelioma and asbestos lawsuit

    When you file a lawsuit, the mass tort attorney who represents you will investigate your allegation and collect evidence that substantiates it. The evidence that makes up your individual or collective lawsuit can include:

    • Medical history
    • Medical bills
    • Employment records
    • Witness statements and affidavits
    • Asbestos expert observations

    In addition to building your case file, your attorney will also identify the at-fault party and conduct interrogatories, depositions, and discovery sessions. He will organize and present your evidence to the at-fault party’s legal and insurance representatives.

    Your lawyer will work toward reaching a settlement agreement that allows you to avoid a prolonged and emotionally trying trial and resolve your case with a favorable financial settlement.

    Recoverable damages in mesothelioma lawsuits

    As with any civil lawsuit, once you prove the at-fault party’s negligence and the connection between their negligence and your injuries, you can pursue them for financial compensation. You can request the following three types of recoverable damages:

    • Economic damages are tangible and fixed expenses. They can include your emergency, ongoing, and long-term medical bills, any assistive medical devices you require, medication costs, and short- and long-term losses of income. Economic damages will also include funeral and burial expenses, where applicable.
    • Non-economic damages are intangible and harder to calculate on your own. They are usually based on the extent of your injury, its length, and your prognosis. They can include physical disabilities, impairments, disfigurement, mental and emotional trauma, and pain and suffering.

    In addition to economic and non-economic damages, you could also be awarded punitive damages. These losses are additional monetary compensation you receive if the at-fault party’s actions are found to be intentional or egregious. Your lawyer will inform you if you qualify for punitive damages.

    Individual and class action lawsuits for mesothelioma

    When you file a lawsuit for the health hazards caused by asbestos exposure, you can file a personal injury lawsuit. If you are the survivor of an employee who became ill or lost their life because of exposure to asbestos that led to a diagnosis of several types of cancers known to be caused by asbestos, you can file a wrongful death lawsuit. Personal injury and wrongful death lawsuits both have their basis in negligence.

    In addition to personal injury and wrongful death cases, there can be two additional types of asbestos lawsuits. If you choose to file an individual lawsuit, you take on the task of identifying the cause of your mesothelioma, assigning financial liability to the at-fault party, and building a case for compensation. An individual lawsuit means you fight back against the identified defendant with no other plaintiffs.

    You can also file a class action lawsuit. When you start such a case, you include others in your pursuit of financial compensation who were injured in a similar fashion and seek damages from the same at-fault party. An attorney will help you determine whether you are eligible to start or join a class action lawsuit with other injured parties.

    Filing an individual lawsuit for asbestos exposure and mesothelioma

    If you became ill or were diagnosed with mesothelioma, lung cancer, or any other form of cancer as the result of asbestos exposure, you may consider filing an individual lawsuit against the at-fault party. When you do so, you bear the full burden of proving your lawsuit.

    Your attorney will guide you through the process of drafting and sending a demand letter with details on your allegations against the defendant and the anticipated value of your lawsuit.

    They can also:

    • Investigate your allegations
    • Assign a value to your case
    • Comply with the statute of limitations
    • Negotiate a financial settlement
    • Represent you in court, if necessary

    In addition, when you file an individual lawsuit, you and your attorney will need to obtain the evidence that supports your case. You also pay the costs associated with the filing of your lawsuit alone. That can include attorney’s fees, which can mean flat rates, billable hours, contingency fees, and/or other expenses.

    Class action lawsuits involving mesothelioma

    Because so many people suffer from asbestos-related types of cancers and other illnesses, they might have been injured by the same entity you cite for your injuries. If that happens, you have the option of starting or joining a class action lawsuit. In accordance with Federal Rules of Civil Procedure Rule 23 guidelines, a class action lawsuit must meet the following pre-qualifying criteria:

    • The number of plaintiffs in the case makes individual lawsuits impractical.
    • All plaintiffs in the case have common “questions of law or fact.”
    • All plaintiffs in the case have similar claims against the at-fault party.
    • All plaintiffs will be fairly represented, and their interests will be fairly protected.

    Discovering that a large number of people have the same physical, financial, and legal complaint you have means you can band together to seek monetary compensation from the at-fault party. When multiple plaintiffs unite in a class action case, an attorney can help you understand the process, how each party shares the costs of the lawsuit, and how you can recover financial compensation.

    Wrongful death lawsuits for mesothelioma

    You have the basis of a wrongful death lawsuit if negligence led to the loss of a family member. The at-fault party’s negligence means they did not provide your loved one with the degree of protection they were due. So, you or other family members may be entitled to financial recovery. To prove you are entitled to compensation in an asbestos lawsuit, you must be able to:

    • Prove an asbestos-related medical condition caused your loved one’s demise
    • Identify which family members are eligible to seek compensation (eligibility may vary by state)
    • Identify and assign financial liability to the correct at-fault party

    When a lawyer represents you in your wrongful death case, he will explain each step involved in the compensation process and help you identify the company that negligently manufactured, sold, or installed products that contained asbestos.

    When building your lawsuit, mesothelioma lawyers will also help you draft a complaint, conduct discovery sessions, hold depositions, and weigh settlement offers. If your case cannot be settled out of court, your lawyer will prepare your case for court.

    Eligibility to file a mesothelioma lawsuit

    Anyone who was in contact with asbestos without being warned about its dangers or without being informed that products they handled contained asbestos can seek financial compensation. According to Mayo Clinic, your personal exposure to dangerous asbestos fibers can lead to adverse health. Asbestos can cause your cells to mutate, multiply, and form cancer cells and tumors.

    Similarly, sharing a home with someone who was exposed to asbestos can also lead to adverse health. You may be eligible to file a lawsuit if you are a:

    • Man or woman who was exposed to asbestos and asbestos fibers at work
    • U.S. veteran who was exposed to asbestos during your military service
    • Person who was injured as the result of second-hand contact with asbestos

    You may have been vulnerable to asbestos as a construction worker, home remodeler, general contractor, subcontractor, or in a host of additional careers. If you believe your asbestos exposure led to your being diagnosed with mesothelioma, a mesothelioma lawsuit lawyer can help you prove it and show you how to file an individual or class action case against the asbestos company.

    Deadline to file a mesothelioma and asbestos lawsuit

    The lawsuit you file for asbestos-related mesothelioma can be a personal injury or wrongful death case. It can also be a single or multiple plaintiff lawsuit. Whichever type of lawsuit you file, you will have a mandatory filing deadline. Every type of civil lawsuit has a time limit commonly called the statute of limitations.

    In general, one of the following statutory filing deadlines will apply to your lawsuit:

    • A personal injury statute of limitations will define the filing deadline for individuals suffering from asbestos exposure and subsequently diagnosed with mesothelioma.
    • A wrongful death statute of limitations will define the filing deadline for family members who lost a loved one due to asbestos-related mesothelioma.

    Once the relevant statute of limitations for your state has been determined, it can still vary according to:

    • The date you were diagnosed with mesothelioma
    • The date of a loved one’s asbestos-related demise
    • The age of the injured party 

    Failing to have your lawsuit filed in time to comply with the statute of limitations could mean you inadvertently relinquish the ability to file at all and you could be left with no legal avenue to compel the at-fault party to compensate you or your family.

    When you work with a network of attorneys, they will explain the many different factors that could potentially alter the statute of limitations in your case.

    Working with a mesothelioma lawyer

    Filing mesothelioma lawsuits for financial compensation after you are diagnosed with mesothelioma or after a loved one succumbs to it can be a complex and arduous process. 

    On your own, the legal parameters and complexities can be daunting. When a lawyer represents you in your pursuit of compensation, he will:

    • Clarify your legal position
    • Identify the at-fault party
    • Organize and submit your evidence
    • Comply with the statute of limitations
    • Build a compelling case file
    • Negotiate a favorable settlement
    • Review the compensation process step by step
    • Explain the merits of individual and class action lawsuits

    When you decide to pursue the at-fault party for monetary recovery, the lawyer you choose to handle your case is important. Because mesothelioma lawsuits can be emotionally charged, look for an attorney who serves his clients with kindness and compassion. Some additional factors to consider when choosing an attorney to represent you include:

    • Their area of specialization
    • Their professional reputation 
    • Their client communication efforts

    Your attorney should provide you with regular updates on the progress of your case. Look for a law firm that offers free reviews and consultations on your case and will accept your case on a contingency-fee basis. This type of fee agreement means you don’t pay out of pocket for attorney’s fees because your lawyer is only paid after your case is settled.

    Steps involved in filing a mesothelioma lawsuit

    Organizing and preparing your case can be an elaborate and involved process. It can include long periods of investigation, mountains of paperwork and documentation, numerous interviews and consultations, and assessing the potential value of your case. 

    In an asbestos lawsuit, you—and others if yours is a class action case—are the plaintiff, and the company from whom you seek monetary compensation is the defendant. When you pursue an asbestos manufacturer, your attorney will draft a letter of complaint and send it to the defendant. The defendant, then, has a limited amount of time — typically 30 days—to respond to the letter.

    Additional steps in building your case can include:

    • Investigating your mesothelioma or asbestos lung cancer
    • Reading and reviewing your medical evidence
    • Identifying and consulting expert witnesses
    • Filing a formal complaint against the at-fault party
    • Conducting discovery sessions and taking depositions

    The discovery process is an important part of your case because it allows your attorney to question the defendant in writing. It also means they can request documentation, evidence, and witness lists that may aid them in building your case.

    Will a mesothelioma lawsuit go to trial?

    The outcome of your personal injury, wrongful death, individual, or class action lawsuit varies depending on whether or not an agreeable financial settlement can be reached. Your case can be resolved with a financial settlement from the at-fault party or their insurance provider.

    A settlement means you agree to accept a specified amount of money to conclude your case instead of proceeding to trial. A settlement is usually the preferred case resolution. Because you, not your attorney, make the final decision to accept or reject a settlement offer, the timeline of settling your case is often up to you.

    If a settlement cannot be reached, your case will proceed to trial. At trial, attorneys for each side will present their case to a judge or jury who will decide which side prevails. 

    If your case is successful, the judge or jury will then decide on the financial damages you receive. Often, the defendant will appeal your victory, which can delay payment of your financial award.

    If your initial lawsuit is unsuccessful, part of preparing your case can also involve filing an appeal. When you pursue the at-fault party for compensation, the lawyer that handles your case will walk you through each step of the preparation process. He will provide explanations and clarity around legal principles and statutes as well as their specific applications to your case.

    Examples of verdicts in mesothelioma lawsuits

    According to RAND Institute for Civil Justice (ICJ) research, asbestos litigation is the longest-running mass tort litigation in the history of the country. This long history of asbestos litigation causes concern among many recent victims of asbestos exposure. Their concerns include worries that asbestos companies may file for bankruptcy or that funds will otherwise not be available to future claimants.

    ICJ’s study of asbestos litigation goes back to the early 1980s and continues into the 2000s. Their research indicates that the number of claims continues to increase for asbestos-related cancer cases and for non-malignant cases. They also cite mesothelioma as a “signature disease” of asbestos exposure. 

    Attorneys can fight for the financial compensation you deserve. Some notable asbestos lawsuit verdicts include:

    • $137 million awarded in the first class-action asbestos-related lawsuit
    • $250 million to a former employee of U.S. Steel Corporation
    • $18.6 million award for the family of a deceased tire builder
    • $16.67 million verdict for the family of a past paper mill employee

    Further research from Reuters cites the average payout in asbestos lawsuits. The average payout for:

    • 2009 was $6.3 million 
    • 2010 was $17.6 million
    • 2011 was $10.5 million 

    As the number of individual and mass tort asbestos injury lawsuits continued to increase over the years, asbestos companies opted to settle cases rather than go to court. Your attorneys should work to settle your mass tort case so that you can get the compensation you and your family deserve.

    Just as people injured by asbestos exposure will experience a wide range of symptoms and illnesses, they will also have a wide range of financial damages. Calculating your recoverable damages on your own can be difficult. Your attorneys will help you understand how to assign a monetary value to your case.

    Get help from an asbestos lawsuit lawyer

    If you or a loved one developed mesothelioma or other forms of cancer due to dangerous asbestos exposure, complete our contact form for help getting started with your asbestos lawsuit.