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.
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.
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
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.
Sports Betting Addiction Lawsuit Sports betting addiction lawsuits are being investigated for college students and young adults who developed gambling problems after using apps like FanDuel and DraftKings, alleging that the platforms failed to warn about the addictive nature of their features and marketing practices.
Ethicon Physiomesh Bellwether Lawsuit To Go Before MDL Jury in December 2019 October 16, 2018 Austin Kirk Add Your CommentsThe U.S. District Judge presiding over all federal hernia mesh lawsuits involving problem with Ethicon Physiomesh indicates that the first “bellwether” case will go before a jury in December 2019, which is designed to help gauge how juries may respond to evidence and testimony that may be repeated throughout hundreds of similar claims.There are currently more than 1,450 product liability lawsuits pending against Johnson & Johnson and it’s Ethicon subsidiary, each raising similar allegations that design defects with Ethicon Physiomesh resulted in painful complications and the need for additional surgery after the surgical mesh failed.The manufacturers issued a global Ethicon Physiomesh recall in May 2016, removing the product from the market amid reports of abdominal pain, infection, hernia recurrence, adhesions, perforations, erosion and failure of the mesh.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 COMPENSATIONGiven similar questions of fact and law raised in complaints filed throughout the federal court system, the cases are centralized for pretrial proceedings before U.S. District Judge Richard Story in the Northern District of Georgia, as part of an MDL, or multidistrict litigation.To reduce duplicative discovery into common issues in the cases, avoid conflicting rulings from different courts and to serve the convenience of parties, witnesses and the judicial system, cases filed in U.S. District Courts nationwide are consolidated before Judge Story for coordinated discovery and a series of early โbellwetherโ trials, which will test the relative strengths and weaknesses of the cases.Judge Story previously established a bellwether process, where a small group of representative claims are going through case-specific discovery, which will be eligible for the first trial dates.According to a practice and procedure order (PDF) issued on October 10, the first Ethicon Physiomesh bellwether lawsuit will go before a jury on December 2, 2019.The order calls for the parties to each select five cases to serve as part of a trial pool, for a total of 10 claims. Plaintiffs’ expert disclosures and reports in those cases will then be served by May 1, 2019, and all expert discovery for trial pool cases should be completed by August 15, 2019.By July 29, 2019, the Court will determine the manner and timing of the trials, as well as the order of selection for plaintiffs. Daubert motions challenging the admissibility of expert witness testimony must be filed by August 28, 2019, and the first trial will be held in December 2019.While the outcome of the bellwether trials is not binding on other plaintiffs involved in the litigation, the cases are being closely watched, as they may influence eventual negotiations to resolve claims.Johnson & Johnsonโs Ethicon unit introduced Physiomesh in March 2010, containing an absorbable film coating on each side of a polypropylene hernia mesh, which was designed to help the patch incorporate into the body and minimize inflammation. However, theย hernia mesh was recalled and removed from the market amid a higher-than-expected number of individuals required revision surgery due to problems with the design.As individuals nationwide contact hernia mesh lawyers after experiencing complications with Ethicon Physiomesh, the size and scope of the litigation is expected to continue to increase over the next few years.Following the coordinated proceedings in the MDL, if Ethicon fails to reachย hernia mesh settlementsย for individuals who had a Physiomesh patch fail, each individual complaint may be transferred back to the U.S. District Court where it originally would have been filed for a future trial date. Tags: Ethicon, Hernia, Hernia Mesh, Johnson & Johnson, Physiomesh Image Credit: |More Hernia Mesh Lawsuit Stories Covidien ProGrip Mesh Complications Lawsuit Filed Over Alleged Defects and Failure To Warn Patients April 21, 2026 Lawsuit Claims Covidien Hernia Mesh Perforated Manโs Bowel April 3, 2026 Parietex ProGrip Hernia Mesh Lawsuit Claims Product Defects Caused Severe Pain After Implantation March 25, 2026 0 Comments PhoneThis field is for validation purposes and should be left unchanged.Share Your CommentsFirst Name*Last NameEmail* Shared Comments*This field is hidden when viewing the formI authorize the above comments be posted on this page Yes NoPost Comment I authorize the above comments be posted on this pageWeekly Digest Opt-In Yes, send me a weekly email with the latest lawsuits, recalls and warnings.Want your comments reviewed by a lawyer?To have an attorney review your comments and contact you about a potential case, provide your contact information below. 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 Abbott Spinal Cord Stimulator Problems Resulted in Severe Paralysis: Lawsuit (Posted: today)A man who became paralyzed has filed an Abbott spinal cord stimulator lawsuit after the original device failed, causing him to suffer electric shocks.MORE ABOUT: SPINAL CORD STIMULATOR LAWSUITAbbott Eterna Lawsuit Alleges Spinal Cord Stimulator Malfunction Resulted in Worsening Pain (05/13/2026)Nevro Stimulator Lawsuit Alleges SCS Lead Failure Caused Nerve Damage (05/06/2026)Lawsuit Claims Abbott, Boston Scientific SCS Pre-Market Approval Supplements Caused Permanent Injuries (04/29/2026) Depo-Provera Lawsuit Filings Exceed 6,000, As Court Prepares for First Test Trials (Posted: yesterday)The number of Depo-Provera lawsuits continues to climb, with more than 6,000 claims now filed nationwide by women who allege they developed brain tumors after receiving the birth control injections.MORE ABOUT: DEPO-PROVERA LAWSUITIntracranial Meningioma from Depo-Provera Shots Caused Hearing Loss, Vision Loss: Lawsuit (05/12/2026)Lawsuit Blames Depo Shot for Brain Tumors, Intense Headaches (04/28/2026)Depo-Provera Meningioma Warning Update Should Be Added to Birth Control Shot: Lawsuit (04/22/2026) SmartPort Surgery Lawsuit Claims AngioDynamics Catheter Fractured Inside Womanโs Body (Posted: 4 days ago)A Missouri woman alleges her AngioDynamics SmartPort catheter fractured and left a broken piece near her heart, requiring surgical removal after it was found during a CT scan.MORE ABOUT: ANGIODYNAMICS PORT CATHETER LAWSUIT18 AngioDynamics Port Catheter Lawsuits Will Be Selected for Bellwether Discovery in August 2026 (05/05/2026)AngioDynamics Catheter Lawsuit Claims SmartPort Device Embedded in Jugular Vein, Caused Embolism (04/30/2026)Vortex Port Lawsuit Filed After Port Catheter Removed Due to Infection, Blood Clots (04/09/2026)
Covidien ProGrip Mesh Complications Lawsuit Filed Over Alleged Defects and Failure To Warn Patients April 21, 2026
Parietex ProGrip Hernia Mesh Lawsuit Claims Product Defects Caused Severe Pain After Implantation March 25, 2026
Abbott Spinal Cord Stimulator Problems Resulted in Severe Paralysis: Lawsuit (Posted: today)A man who became paralyzed has filed an Abbott spinal cord stimulator lawsuit after the original device failed, causing him to suffer electric shocks.MORE ABOUT: SPINAL CORD STIMULATOR LAWSUITAbbott Eterna Lawsuit Alleges Spinal Cord Stimulator Malfunction Resulted in Worsening Pain (05/13/2026)Nevro Stimulator Lawsuit Alleges SCS Lead Failure Caused Nerve Damage (05/06/2026)Lawsuit Claims Abbott, Boston Scientific SCS Pre-Market Approval Supplements Caused Permanent Injuries (04/29/2026)
Depo-Provera Lawsuit Filings Exceed 6,000, As Court Prepares for First Test Trials (Posted: yesterday)The number of Depo-Provera lawsuits continues to climb, with more than 6,000 claims now filed nationwide by women who allege they developed brain tumors after receiving the birth control injections.MORE ABOUT: DEPO-PROVERA LAWSUITIntracranial Meningioma from Depo-Provera Shots Caused Hearing Loss, Vision Loss: Lawsuit (05/12/2026)Lawsuit Blames Depo Shot for Brain Tumors, Intense Headaches (04/28/2026)Depo-Provera Meningioma Warning Update Should Be Added to Birth Control Shot: Lawsuit (04/22/2026)
SmartPort Surgery Lawsuit Claims AngioDynamics Catheter Fractured Inside Womanโs Body (Posted: 4 days ago)A Missouri woman alleges her AngioDynamics SmartPort catheter fractured and left a broken piece near her heart, requiring surgical removal after it was found during a CT scan.MORE ABOUT: ANGIODYNAMICS PORT CATHETER LAWSUIT18 AngioDynamics Port Catheter Lawsuits Will Be Selected for Bellwether Discovery in August 2026 (05/05/2026)AngioDynamics Catheter Lawsuit Claims SmartPort Device Embedded in Jugular Vein, Caused Embolism (04/30/2026)Vortex Port Lawsuit Filed After Port Catheter Removed Due to Infection, Blood Clots (04/09/2026)