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.
Bard Opposes Remanding Hernia Mesh Lawsuits, Indicating Fourth Bellwether Trial Should Move Forward in MDLManufacturer indicates that a final Bard hernia mesh bellwether trial should go forward in April 2024, before the Court considers any remand process. January 26, 2024 Irvin Jackson Add Your CommentsC.R. Bard is asking the U.S. District Judge presiding over all federal Bard hernia mesh lawsuits to delay sending cases back to their originating courts for trial, indicating that it remains premature, even though the parties have failed to negotiate global settlements more than five years after all claims were consolidated as part of a multidistrict litigation (MDL).Nearly 21,000 product liability lawsuits have been filed against C.R. Bard throughout the federal court system, each involving similar allegations that users suffered painful and debilitating injuries caused by design defects associated with various polypropylene products sold in recent years, including the Bard Ventralight, Bard Ventralex, Bard Perfix Plug, Bard 3DMax, and other similar systems.Since each of the claims raise similar questions of fact and law, the hernia mesh lawsuits have been centralized before U.S. District Judge Edmund A. Sargus in the Southern District of Ohio since August 2018, as part of a federal Bard hernia mesh MDL, where the parties have already held three test trials to help determine how juries may respond to certain evidence and testimony that may be repeated throughout the claims.Although the bellwether trials were designed to promote resolution of the litigation, large numbers of Bard hernia mesh settlements have not materialized, and thousands of individuals are still awaiting their day in court.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 COMPENSATIONJudge Sargus presided over the first Bard hernia mesh trial in August 2021, which resulted in a ย defense verdict for Bard, following lengthy delays due to the COVID-19 pandemic. However, a second bellwether trial followed in April 2022, resulting in aย $255,000 verdict, and the third resulted in aย $500,000 verdictย in November 2023.In August 2022, a state court lawsuit in Rhode Island ended with aย $4.8 million verdict over Bard Ventralex mesh problems, which sent a strong signal to the manufacturer about the extent of liability it may face if each of the remaining cases goes before a jury.With a fourth andย final Bard hernia mesh bellwether trial scheduled to go before a jury in April 2024, involving complications with Bard 3DMax, the Plaintiffs Steering Committee (PSC) filed a motion last month calling for the court to start planning for the remand of Bard hernia mesh lawsuits back to the U.S. District Courts where they originated.Bard Opposes Remand of Hernia Mesh LawsuitsPlaintiffs maintain that the pretrial proceedings in the MDL have essentially been completed, with the Court making it clear the fourth bellwether trial in April would be the last.To help move cases forward, the PSC asked Judge Sargus to identify a group of 1,500 cases, representing approximately 7.5% of all cases filed in the MDL, and return those cases to U.S. District Courts nationwide so that lawyers could begin preparing for large numbers of trials to determine the amount of damages they are entitled to receive.Earlier this week, Bard filed a response (PDF) opposing any remand process at this point, calling it โpremature, unreasonable, and counter-productiveโ.The defendants argue that remand should not be considered until after the fourth bellwether trial, which it says will be important in evaluating the entire litigation and determining the next steps.Bard notes that the litigation is unusual in that it involves more than 20 different medical devices, some dating back to the early 1960s, and almost all of which are currently still on the market. The manufacture indicates that this made it impossible to reach a resolution based on the merits of each individual device. The defendantsโ response indicates it is important to hold the fourth bellwether trial before remand talks begin so that the parties can look at the results from as broad a range of devices as possible.The response indicates that the four devices represented in the bellwether trials, the Ventralight ST, Ventralex, PerFix Plug and 3DMax, represent more than half the devices used in the pending cases.โWhile Bard agrees that core discovery is substantially complete and that the bellwether process and trials have provided useful information for both possible resolution of cases and the eventual trials of cases in transferee courts, Bard disagrees that it is time to abandon the bellwether process and the fourth trial,โ the response states. โViewing the course of the litigation as a whole, including patterns of filings, the Courtโs rulings, and the juriesโ verdicts, it makes sense to stay the course and assess where things stand after the bellwether process is completed.โThe Plaintiffsโ Steering Committee has 10 days to respond to this opposition.While the outcome of the early bellwether trials have no binding impact on other claims, facing the prospect of hundreds of individual claims going before juries in different U.S. District Courts nationwide will increase pressure on the manufacturer to negotiate hernia mesh settlements to resolve large groups of claims.The next case management conference will be held on February 6. 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: 3DMax, Bard Perfix Plug, C. R. Bard, Hernia, Hernia Mesh, Ventralex, Ventralight Image Credit: |More Hernia Mesh Lawsuit Stories Covidien Mesh Lawsuit Cleared for Trial Over Hernia Repair Complications June 10, 2026 Bard Ventralight Lawsuit Claims Hernia Mesh Failure Resulted in Ongoing Physical Disabilities June 3, 2026 Bard Ventralex Patch Lawsuit Claims Umbilical Hernia Mesh Failed, Requiring Removal Surgery May 21, 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 Covidien Mesh Lawsuit Cleared for Trial Over Hernia Repair Complications (Posted: today)A Covidien hernia mesh lawsuit will go before a jury next month after a federal judge rejected the manufacturer’s motion to have the case dismissed.MORE ABOUT: HERNIA MESH LAWSUITBard Ventralight Lawsuit Claims Hernia Mesh Failure Resulted in Ongoing Physical Disabilities (06/03/2026)Bard Ventralex Patch Lawsuit Claims Umbilical Hernia Mesh Failed, Requiring Removal Surgery (05/21/2026)Covidien ProGrip Mesh Complications Lawsuit Filed Over Alleged Defects and Failure To Warn Patients (04/21/2026) Olympus Endoscope Lawsuit Filed Over ERCP Infection, Sepsis Linked to Contaminated Scope (Posted: yesterday)Lawsuit alleges Olympus failed to address known problems with sterilizing duodenoscopes, leading to a fatal ERCP infection years after federal regulators first raised concerns about the devices.MORE ABOUT: SCOPE INFECTION LAWSUITPediatric Sepsis Cases Contribute to More Than 1,800 Childrenโs Deaths Annually in U.S.: Study (03/31/2026)Infections After Colonoscopy, ERCP May Result in Lawsuits Over Olympus Scope Problems (03/27/2026) Boston Scientific Stimulator Lawsuits Centralized in Federal MDL (Posted: 2 days ago)Federal regulators have centralized at least 23 Boston Scientific spinal cord stimulator lawsuits in a multidistrict litigation that excludes multiple similar claims involving Abbott and Nevro implants.MORE ABOUT: SPINAL CORD STIMULATOR LAWSUITLawsuit Indicates Spinal Cord Stimulator Lead Complications Resulted in Shocks, Removal Surgery (06/02/2026)Spinal Cord Stimulator Malpractice Lawsuit Claims Device Left Veteran Partially Paralyzed (05/29/2026)Abbott Spinal Cord Stimulator Problems Resulted in Severe Paralysis: Lawsuit (05/19/2026)
Bard Ventralight Lawsuit Claims Hernia Mesh Failure Resulted in Ongoing Physical Disabilities June 3, 2026
Bard Ventralex Patch Lawsuit Claims Umbilical Hernia Mesh Failed, Requiring Removal Surgery May 21, 2026
Covidien Mesh Lawsuit Cleared for Trial Over Hernia Repair Complications (Posted: today)A Covidien hernia mesh lawsuit will go before a jury next month after a federal judge rejected the manufacturer’s motion to have the case dismissed.MORE ABOUT: HERNIA MESH LAWSUITBard Ventralight Lawsuit Claims Hernia Mesh Failure Resulted in Ongoing Physical Disabilities (06/03/2026)Bard Ventralex Patch Lawsuit Claims Umbilical Hernia Mesh Failed, Requiring Removal Surgery (05/21/2026)Covidien ProGrip Mesh Complications Lawsuit Filed Over Alleged Defects and Failure To Warn Patients (04/21/2026)
Olympus Endoscope Lawsuit Filed Over ERCP Infection, Sepsis Linked to Contaminated Scope (Posted: yesterday)Lawsuit alleges Olympus failed to address known problems with sterilizing duodenoscopes, leading to a fatal ERCP infection years after federal regulators first raised concerns about the devices.MORE ABOUT: SCOPE INFECTION LAWSUITPediatric Sepsis Cases Contribute to More Than 1,800 Childrenโs Deaths Annually in U.S.: Study (03/31/2026)Infections After Colonoscopy, ERCP May Result in Lawsuits Over Olympus Scope Problems (03/27/2026)
Boston Scientific Stimulator Lawsuits Centralized in Federal MDL (Posted: 2 days ago)Federal regulators have centralized at least 23 Boston Scientific spinal cord stimulator lawsuits in a multidistrict litigation that excludes multiple similar claims involving Abbott and Nevro implants.MORE ABOUT: SPINAL CORD STIMULATOR LAWSUITLawsuit Indicates Spinal Cord Stimulator Lead Complications Resulted in Shocks, Removal Surgery (06/02/2026)Spinal Cord Stimulator Malpractice Lawsuit Claims Device Left Veteran Partially Paralyzed (05/29/2026)Abbott Spinal Cord Stimulator Problems Resulted in Severe Paralysis: Lawsuit (05/19/2026)