Scope Infection Lawsuit Patients across the United States have filed medical scope infection lawsuits after contaminated endoscopes and duodenoscopes allegedly transmitted dangerous bacterial infections during procedures such as ERCP, colonoscopy, and other endoscopic treatments.
Spinal Cord Stimulator Lawsuit Spinal cord stimulator lawsuits allege that implanted pain devices malfunctioned, migrated, or caused nerve damage, often forcing patients to undergo revision or removal surgery.
Depo-Provera Lawsuit Depo-Provera lawsuits are being investigated for women who developed meningioma brain tumors after receiving Depo-Provera birth control shots, claiming that Pfizer failed to adequately disclose side effects.
Chlorpyrifos Parkinsonโs Disease Lawsuit Chlorpyrifos lawsuits are being investigated for individuals diagnosed with Parkinsonโs disease after direct, residential, occupational or Gulf War pesticide exposure.
Ozempic Lawsuit Lawyers are pursuing Ozempic lawsuits, Wegovy lawsuits and Mounjaro lawsuits over gastroparesis or stomach paralysis, which can leave users with long-term gastrointestinal side effects
Suboxone Tooth Decay Lawsuit Lawsuits are being pursued by users of Suboxone who experienced tooth loss, broken teeth or required dental extractions. Settlement benefits may be available.
Hair Relaxer Lawsuit Regular exposure to chemicals in hair relaxer may cause uterine cancer, ovarian cancer and other injuries. Women diagnosed with cancer may be eligible for settlement benefits.
Nitrous Oxide Lawsuit Individuals who suffered harm, or families who lost a loved one after using nitrous oxide products may be eligible for financial compensation through a nitrous oxide lawsuit.
Breast Mesh Lawsuit Lawyers are investigating breast mesh lawsuits for women who suffered infections, pain, or implant failure from internal bra implants used in breast reconstruction surgery.
Bard PowerPort Lawsuit Serious and life-threatening injuries have been linked to problems with Bard PowerPort. Lawsuits are now being pursued by individuals who suffered injuries from the implantable port catheter fracturing or migrating.
MDL Sought for Covidien Mesh Lawsuits As Number of Claims Is “Beginning to Balloon”The JPML rejected a request to consolidate the cases in 2020, at which time there were only 12 Covidien mesh lawsuits filed. Now that number has increased to 73, with thousands of additional claims expected. February 22, 2022 Irvin Jackson Add Your CommentsThe medical device manufacturer Covidien has renewed a motion to consolidate and centralize all hernia mesh lawsuits it will face throughout the federal court system, indicating that thousands of claims may ultimately be presented by individuals who have experienced problems with Covidien Parietex, Covidien Symbotex and similar products.The U.S. Judicial Panel on Multidistrict Litigation (JPML) previously rejected a request to establish a Covidien mesh MDL in June 2020, finding that there were too few cases pending at that time to justify formal pretrial proceedings in the federal court system. However, the manufacturer now indicates that the number of claims “are indeed beginning to balloon”, with at least 73 lawsuits pending in seven different U.S. District Courts.Each of the claims raise similar questions of fact and law, leading the manufacturer to ask that the litigation be centralized before one U.S. District Judge to prevent duplicative discovery into common issues in the claims, avoid conflicting pretrial rulings and to promote judicial efficiencies.Hernia Mesh LawsuitsDid you or a loved one receive a hernia mesh?Hernia mesh lawsuits are being filed against Bard, Atrium, Covidien and several other hernia mesh manufacturers over mesh failures resulting in injuries and additional surgery.Learn MoreSEE IF YOU QUALIFY FOR COMPENSATIONHernia Mesh LawsuitsDid you or a loved one receive a hernia mesh?Hernia mesh lawsuits are being filed against Bard, Atrium, Covidien and several other hernia mesh manufacturers over mesh failures resulting in injuries and additional surgery.Learn MoreSEE IF YOU QUALIFY FOR COMPENSATIONIn a memorandum of law (PDF) filed in support of it’s new motion on February 18, Covidien indicates that it was unable to disclose in 2020 that tolling agreements were in place with more than 6,000 potential claimants, who had agreed to hold off on filing lawsuits while the parties attempted to negotiate hernia mesh settlements. However, as the tolling agreements expire, complaints are being filed in state and federal courts nationwide at a rapid rate.In addition to the federal litigation, at least 4,700 Covidien mesh lawsuits have been brought in Massachusetts state court, where the manufacturer’s U.S. headquarters are located. However, Covidien indicates that the vast majority of plaintiffs in those cases do not reside in Massachusetts and it intends to seek dismissal of the state court claims, which may result in many of those cases being refiled in the federal court system.“If the Massachusetts court grants that motion, hundreds more cases will be refiled in federal court (or, if re-filed in state court, will be subject to removal based on diversity of citizenship),” according to the manufacturer. “These cases would be only a few strides out of the starting blocks: written discovery still being exchanged in the coordinated Massachusetts proceeding, and no depositions have been taken.”In complex product liability litigation, where a large number of claims are filed throughout the federal court system by individuals who suffered similar injuries as a result of the same or similar products, it is common for the federal court system to centralize the litigation for pretrial proceedings.Covidien is asking that all of the hernia mesh cases currently pending or brought in the future throughout the federal courts be transferred to the U.S. District Court for the District of Massachusetts, where all but six current cases are already being pursued.At least three other hernia mesh MDLs are already established for claims involving other polyethylene products, with more than 15,400 Bard hernia mesh lawsuits centralized in the Southern District of Ohio, 3,600 Ethicon Physiomesh lawsuits centralized in the Northern District of Georgia and 3,251 Atrium C-Qur lawsuits centralized in the District of New Hampshire.If consolidation is approved for the Covidien mesh lawsuits, it is expected that the U.S. District Judge appointed to preside over the proceedings will select a small group of representative “bellwether” cases for early trial dates, to help gauge how juries are likely to respond to certain evidence regarding the alleged design defects with the Covidien products. While the outcomes of these bellwether trials will not be binding on other plaintiffs, they may help drive the parties toward settlements that would avoid the need for hundreds of individual trials to be held. Written by: Irvin JacksonSenior Legal Journalist & Contributing EditorIrvin Jackson is a senior investigative reporter at AboutLawsuits.com with more than 30 years of experience covering mass tort litigation, environmental policy, and consumer safety. He previously served as Associate Editor at Inside the EPA and contributes original reporting on product liability lawsuits, regulatory failures, and nationwide litigation trends. Tags: Covidien, Hernia Mesh, Medtronic, ParietexMore Hernia Mesh Lawsuit Stories Covidien Mesh Lawyers to Meet With MDL Judge This Week, Following Landmark Verdict August 17, 2026 Covidien Hernia Mesh Lawsuit Payout of $88M Awarded in First MDL Bellwether Trial August 5, 2026 Hernia Mesh Failure Lawsuit Alleges ProGrip Implant Was Prone to Breaking and Fragmenting August 3, 2026 1 Comments Stephen April 9, 2022 I’ve suffered from symbotex mesh implanted in may 2018 injury on job repaired by company doctor,I’ve had many side effects and complications, inflammation,chronic pain,hernia reoccurrence,bowel obstruction that resulted in 7 days in hospital from surgery emergency nearly lost my life,pertinitis from mesh,and joint pain…this has impacted my life and I can’t get anyone to help for no recall or revision surgery!! Why doesn’t the FDA recall I know I’m not the only one due compensation..??!! 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This will not be published.Contact Phone #Alt Phone #Private CommentsNOTE: Providing information for review by an attorney does not form an attorney-client relationship.CAPTCHAGA SourceGA CampaignGA MediumGA ContentGA TermΔ MORE TOP STORIES Dupixent Lymphoma Lawsuit Alleges Atopic Dermatitis Drug Led to Mycosis Fungoides Diagnosis (Posted: today)A California woman’s Dupixent lymphoma lawsuit claims the manufacturers knew of the eczema drug’s cancer risks, but refused to inform doctors and patients.MORE ABOUT: DUPIXENT LAWSUITDupixent CTCL Studies Highlighted Cancer Risks For Years, Lawsuit Alleges (08/11/2026)CTCL Lawsuit Alleges Diagnosis Came After Less Than a Year of Dupixent Use (07/29/2026)Lawsuit Alleges Dupixent Caused Mycosis Fungoides Diagnosis (07/21/2026) FanDuel Addiction Lawsuit Alleges Targeted Advertising Caused Substantial Gambling Losses (Posted: yesterday)A FanDuel addiction lawsuit claims a Pennsylvania man wagered massive amounts of money after being subjected to a tailored promotional campaign designed to exploit his gambling habits.MORE ABOUT: SPORTS BETTING ADDICTION LAWSUITDraftKings Predictions Lawsuit Seeks Refunds for Illegal Sports Betting Losses (08/11/2026)Class Action Lawsuit Claims DraftKings Is Dodging State Gambling Laws (07/31/2026)Lawsuit Claims FanDuel, DraftKings Caused Compulsive Gambling, Addiction and Financial Losses (07/24/2026) Boston Scientific Stimulator Lawsuit Alleges Spine Implant Caused Nerve Damage, Shocks (Posted: 2 days ago)A spinal cord stimulator lawsuit from a Kentucky man claims his Boston Scientific device was defectively designed, leaving him with permanent nerve damage and wire fragments fused into his bones.MORE ABOUT: SPINAL CORD STIMULATOR LAWSUITNevro Stimulator Lawsuit MDL Request Opposed by Manufacturer (08/14/2026)Abbott Continues to Oppose Spinal Cord Stimulator Lawsuit MDL, Despite Mounting Claims (08/10/2026)Lawsuit Over Spinal Cord Stimulator Removal Claims Device Caused Numbness, Incontinence (08/06/2026)
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