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 MDL Manufacturer 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 Comments C.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 Lawsuits Did 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 More SEE IF YOU QUALIFY FOR COMPENSATION Hernia Mesh Lawsuits Did 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 More SEE IF YOU QUALIFY FOR COMPENSATION Judge 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 Lawsuits Plaintiffs 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.โ The 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 Jackson Senior Legal Journalist & Contributing Editor Irvin 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 Parietex ProGrip Hernia Mesh Lawsuit Claims Product Defects Caused Severe Pain After Implantation March 25, 2026 MDL Trial for Covidien Hernia Mesh Lawsuit Remains On Track for July 2026 March 2, 2026 Covidien ProGrip Hernia Mesh Lawsuit Joins Over 2,200 Similar Claims in MDL January 9, 2026 0 Comments NameThis 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 No Post Comment I authorize the above comments be posted on this page Weekly 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 Term Δ MORE TOP STORIES Hair Relaxer Class Action Lawsuit Seeks Certification for Medical Monitoring Claims (Posted: today) A federal judge is being asked to certify seven hair relaxer class action lawsuits seeking medical monitoring for users, following studies that link the products to an increased risk of cancer. 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Parietex ProGrip Hernia Mesh Lawsuit Claims Product Defects Caused Severe Pain After Implantation March 25, 2026
Hair Relaxer Class Action Lawsuit Seeks Certification for Medical Monitoring Claims (Posted: today) A federal judge is being asked to certify seven hair relaxer class action lawsuits seeking medical monitoring for users, following studies that link the products to an increased risk of cancer. MORE ABOUT: HAIR RELAXER LAWSUITHair Relaxer Endometrial Cancer Lawsuits and Ovarian Cancer Lawsuits Proposed for Early Trials (03/23/2026)Lawyers To Nominate Hair Relaxer Cancer Cases for Early Bellwether Trials Next Week (03/12/2026)Court Outlines Procedures When Women Die After Filing a Hair Relaxer Cancer Lawsuit (02/25/2026)
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