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.
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.
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.
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.
AngioDynamics Port Catheter 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.
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.
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.
Dupixent Lawsuit Dupixent lawsuits are being investigated for patients who developed rare blood cancers such as cutaneous T-cell lymphoma (CTCL) after receiving injections, alleging that Sanofi and Regeneron failed to warn about the potential risks of immune suppression and delayed cancer diagnosis.
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.
Stay Issued Pending Settlement of Bard Hernia Mesh Lawsuits in MDL A Bard hernia mesh global settlement is believed to be imminent, however no details on the terms of any pending agreement have been released. July 8, 2024 Irvin Jackson Add Your Comments The U.S. District Judge presiding over all federal Bard hernia mesh lawsuits has issued a limited stay on the active litigation, pausing all discovery and pretrial proceedings, as the parties close in on a potential global settlement agreement to resolve claims brought by individuals nationwide. C.R. Bard currently faces more than 21,000 separate product liability lawsuits, 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 3D Max, and similar systems. Since August 2018, the hernia mesh lawsuits have been centralized before U.S. District Judge Edmund A. Sargus in the Southern District of Ohio, as part of a federal Bard hernia mesh multidistrict litigation, or MDL. Following mixed results in three early bellwether test trials, which were held to help determine how juries may respond to certain evidence and testimony that may be repeated throughout the claims, Judge Sargus ordered the parties to meet with a mediator over the past three months, to conduct intensive Bard hernia mesh settlement talks before he considers returning large numbers of claims to various different U.S. District Courts nationwide for trial. However, based on a series of case management orders issued over the weekend, including docket control measures that impose strict deadlines on any new claims that may be filed in the future, it appears that an agreement on settling Bard hernia mesh claims may soon be announced by the parties. 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 Bard Hernia Mesh Litigation Orders Impose Strict Deadlines On Non-Settling Plaintiffs Following a joint request submitted by the manufacturer and plaintiffs attorneys, Judge Sargus issued a limited stay (PDF) on July 6, pausing all deadlines for any lawsuits filed before the date of the order, indicating that those parties can not take any discovery, file any motions or seek any other relief. Judge Sargus indicated that the stay was announced in anticipation of potential global settlement for Bard hernia mesh lawsuits, suggesting that each individual plaintiff will soon have the ability to determine whether to settle their case or proceed with further litigation of their claim. “The Court anticipates that the stay will be lifted in cases in which the plaintiffs opt-out of the Master Settlement Agreement,” wrote Judge Sargus in the order, indicating that the manufacturer must file an individualized notice in each case where a plaintiff decides not to participate in the settlement, which will then impose a series of strict deadlines for the further litigation. A separate docket control order (PDF) was also issued over the weekend, outlining the requirements that will be imposed on individuals who opt out of the settlement, or file a new lawsuit after July 6, 2024. Among other requirements, those plaintiffs will be required to file a certification under penalty of perjury regarding their ability to pursue a new claim, produce early discovery documents and submit case-specific expert reports that establish their injury was caused by one or more Bard hernia mesh products. Any plaintiffs who fail to comply with the strict deadlines will face dismissal of their claim. 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 More Hernia Mesh Lawsuit Stories Covidien ProGrip Hernia Mesh Lawsuit Joins Over 2,200 Similar Claims in MDL January 9, 2026 Covidien Symbotex Mesh Lawsuit Reset For Trial in July 2026 November 24, 2025 Feb. 2026 Trial for Covidien Hernia Mesh Lawsuit Canceled by MDL Judge November 5, 2025 0 Comments URLThis 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 MDL Sought for Spinal Cord Stimulator Lawsuits Against Abbott, Boston Scientific (Posted: yesterday) Plaintiffs are asking a federal panel to consolidate a growing number of spinal cord stimulator lawsuits against Abbott and Boston Scientific, alleging defective design changes caused lead fractures, device failures and neurological injuries nationwide. MORE ABOUT: SPINAL CORD STIMULATOR LAWSUITBoston Scientific SCS Lawsuit Filed Over Problems With WaveWriter Alpha System (02/16/2026)Lawsuit Claims Spinal Cord Stimulator Battery Problems Resulted in Removal of Boston Scientific Device (02/02/2026)Abbott Eterna Spinal Cord Stimulator Lawsuit Filed Over Lead Migration, Device Malfunction (01/26/2026) Depo-Provera Brain Tumor Risks Make Birth Control Shot Unreasonably Dangerous: Lawsuit (Posted: 4 days ago) A New York woman has filed a lawsuit alleging that her long term use of Depo Provera caused her to develop a meningioma brain tumor, which she contends resulted from the manufacturer’s negligence and failure to adequately warn about the risks. MORE ABOUT: DEPO-PROVERA LAWSUITPfizer Indicates Depo-Provera Meningioma Lawsuits Should Be Preempted by Federal Law (02/03/2026)Proposed Depo-Provera Lawsuit Schedule Calls for First Trial in Dec. 2026 (01/23/2026)Lawsuit Indicates Depo-Provera Meningioma Diagnosis Followed Memory Loss, Dizziness Symptoms (01/20/2026) MDL Sought for Dupixent Lymphoma Lawsuits Filed in Federal Courts Nationwide (Posted: 5 days ago) A group of plaintiffs has petitioned the U.S. Judicial Panel on Multidistrict Litigation to centralize all Dupixent lymphoma lawsuits before a single judge for coordinated pretrial proceedings, a move that could ultimately lead to bellwether trials and a global resolution of the claims. MORE ABOUT: DUPIXENT LAWSUITLawsuit Claims Dupixent for Atopic Dermatitis, Eczema Treatment Caused CTCL (02/10/2026)CTCL Diagnosis Leads to Lawsuit Over Dupixent Cancer Risks (02/03/2026)Lawsuit Claims Dupixent Side Effects Led to CTCL Cancer Diagnosis (01/12/2026)
MDL Sought for Spinal Cord Stimulator Lawsuits Against Abbott, Boston Scientific (Posted: yesterday) Plaintiffs are asking a federal panel to consolidate a growing number of spinal cord stimulator lawsuits against Abbott and Boston Scientific, alleging defective design changes caused lead fractures, device failures and neurological injuries nationwide. MORE ABOUT: SPINAL CORD STIMULATOR LAWSUITBoston Scientific SCS Lawsuit Filed Over Problems With WaveWriter Alpha System (02/16/2026)Lawsuit Claims Spinal Cord Stimulator Battery Problems Resulted in Removal of Boston Scientific Device (02/02/2026)Abbott Eterna Spinal Cord Stimulator Lawsuit Filed Over Lead Migration, Device Malfunction (01/26/2026)
Depo-Provera Brain Tumor Risks Make Birth Control Shot Unreasonably Dangerous: Lawsuit (Posted: 4 days ago) A New York woman has filed a lawsuit alleging that her long term use of Depo Provera caused her to develop a meningioma brain tumor, which she contends resulted from the manufacturer’s negligence and failure to adequately warn about the risks. MORE ABOUT: DEPO-PROVERA LAWSUITPfizer Indicates Depo-Provera Meningioma Lawsuits Should Be Preempted by Federal Law (02/03/2026)Proposed Depo-Provera Lawsuit Schedule Calls for First Trial in Dec. 2026 (01/23/2026)Lawsuit Indicates Depo-Provera Meningioma Diagnosis Followed Memory Loss, Dizziness Symptoms (01/20/2026)
MDL Sought for Dupixent Lymphoma Lawsuits Filed in Federal Courts Nationwide (Posted: 5 days ago) A group of plaintiffs has petitioned the U.S. Judicial Panel on Multidistrict Litigation to centralize all Dupixent lymphoma lawsuits before a single judge for coordinated pretrial proceedings, a move that could ultimately lead to bellwether trials and a global resolution of the claims. MORE ABOUT: DUPIXENT LAWSUITLawsuit Claims Dupixent for Atopic Dermatitis, Eczema Treatment Caused CTCL (02/10/2026)CTCL Diagnosis Leads to Lawsuit Over Dupixent Cancer Risks (02/03/2026)Lawsuit Claims Dupixent Side Effects Led to CTCL Cancer Diagnosis (01/12/2026)