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.
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.
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.
Tabletop Fire Pit Lawsuit Individuals who suffered severe burns, or families who lost a loved one in a tabletop fire pit explosion, may be eligible for financial compensation through a fire pit injury lawsuit.
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.
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.
Ocaliva Lawsuit Ocaliva lawsuits are being investigated for users who experienced liver failure, cirrhosis progression, transplant, or death after taking the drug, alleging that Intercept Pharmaceuticals failed to warn about the risk of dosing toxicity and accelerated liver damage.
Roblox Lawsuit Families are filing Roblox lawsuits after children were targeted by predators for grooming, sextortion, sexual abuse, or exploitation on the platform. Learn who qualifies, what cases allege, and how to file a confidential claim.
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.
Bard Hernia Mesh Lawyers Appointed To Leadership Roles in New MDL September 20, 2018 Austin Kirk Add Your Comments The U.S. District Judge presiding over all federal hernia mesh lawsuits filed against C.R. Bard has appointed a small group of plaintiffs’ lawyers to serve in various leadership roles in the recently established multidistrict litigation (MDL), involving claims brought by individuals nationwide who have experienced problems with various polypropylene mesh designs sold in recent years. Hundreds of product liability lawsuits have been filed throughout the federal court system over complications with Bard Ventralex, Bard Perfix, Bard Composix and other polypropylene hernia patch products sold by C.R. Bard, each raising similar allegations that design defects make the mesh prone to fail and result in the need for revision surgery within a few years. Given similar questions of fact and law raised in the complaints, the U.S. Judicial Panel on Multidistrict Litigation established consolidated pretrial proceedings for the Bard hernia mesh cases last month, centralizing cases filed nationwide before U.S. District Judge Edmund A. Sargus in the Southern District of Ohio, for coordinated discovery and management. 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 As hernia mesh lawyers continue to review and file potential cases for individuals who have experienced problems following a hernia repair in recent years, the size and scope of the litigation is expected to continue to grow, with many estimates suggesting that several thousands lawsuits will ultimately be centralized in the Bard hernia mesh MDL. In a case management order (PDF) issued on September 19, Judge Sargus appointed two attorneys to serve as Plaintiffs’ Co-Lead Counsel, one Plaintiffs’ Liaison Counsel, four to serve on a Plaintiffs’ Executive Committee and eight additional attorneys to serve on a Plaintiff’s Steering Committee. In complex medical device litigation, where a large group of cases present similar claims, it is common for the Court to appoint a group of lawyers to leadership roles to coordinate general discovery into common issues in the cases, argue motions before the court and take certain actions during the MDL proceedings that will benefit all plaintiffs. However, each individual plaintiff will still maintain their own attorney to handle case-specific issues and establish that their injuries were caused by defects associated with the Bard hernia mesh products. As part of the pretrial proceedings, it is expected that Judge Sargus will establish a bellwether process, where a small group of Bard hernia mesh cases will be prepared for early trial dates to help gauge how juries may respond to certain evidence and testimony that is likely to be repeated throughout the litigation. If Bard hernia mesh settlements are not reached following the coordinated MDL proceedings, each case may ultimately be remanded back to the U.S. District Court where it was originally filed for an individual trial date in the future. Hernia Mesh Litigation In addition to Bard lawsuits, similar polypropylene hernia patch cases are being pursued over problems with the Atrium C-Qur patch and Ethicon Physiomesh, which have already been centralized as part of two separate multidistrict litigations (MDLs). The Atrium C-Qur, pronounced “Secure”, was approved by the FDA in March 2006, featuring a polypropylene mesh with an outer coating of gel made from 3 fatty acids. However, this design has been linked to reports of severe infections, allergic reactions and other problems. Ethicon Physiomesh was introduced in March 2010, featuring a unique, multilayered design that was intended to improve performance. However, amid a high number of failures, an Ethicon Physiomesh recall was issued in May 2016, removing the product from the market worldwide. While the action was classified as a “market withdrawal” in the United States, the manufacturer has indicated that it will not be returning the product to the market. There are currently about 1,200 Ethicon Physiomesh lawsuits and 471 Atrium C-Qur lawsuits pending in the federal court system, where they have been centralized before two separate judges for coordinated discovery. Tags: Bard, C. R. Bard, Hernia, Hernia Mesh, Kugel Image Credit: | More Hernia Mesh Lawsuit Stories Covidien Seeks Dismissal of Lawsuits Over Hernia Mesh Complications September 8, 2025 Deadline for Covidien Mesh Settlement Negotiations Extended Until Jan. 2026 August 21, 2025 LifeCell Seeks Dismissal of Strattice Hernia Mesh Lawsuit Set for Trial August 11, 2025 1 Comments Dorothy August 1, 2020 The women with TVM or and Slings with mesh was not advised to have a separate attorney to deal with additional illnesses that were associated with the mesh polypropylene. Biological or Synthetic. Compensation was paid strictly on # of surgeries to remove the mesh when some could never find a doctor that believed in mesh injury or lack the funds to get to one of the few qu a qualified doctors who could remove it .Is it to late to go after the mesh companies for all the lifelong illness from the mesh polypropylene. Not just # of surgeries. And why does FDA walk away untouched after recalling Boston Science but letting the other manufacturers through on 510k . Remember they recalled the only one they approved. CompanyThis 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 Internal Bra Side Effects Raise Questions About Manufacturers’ Knowledge of Mesh Failures (Posted: yesterday) Breast mesh products marketed as “internal bras” for lift and augmentation surgeries are now under investigation amid reports of painful complications, and questions over manufacturers’ prior knowledge of mesh-related risks. MORE ABOUT: BREAST MESH LAWSUITBreast Mesh Problems Prompted FDA Warnings Over Off-Label Use (10/15/2025)Breast Mesh Lawsuits May Follow Recent Studies Highlighting Internal Bra Complications (10/09/2025)FDA Warns BD Surgical Mesh Products Not Proven Safe for Breast Reconstruction Surgery (11/10/2023) Four BioZorb Breast Marker Lawsuits Set for Trial Between Jan. and April 2026 (Posted: 4 days ago) A federal judge has set key scheduling deadlines for the four first bellwether trials over claims that BioZorb breast markers are defectively designed. 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Internal Bra Side Effects Raise Questions About Manufacturers’ Knowledge of Mesh Failures (Posted: yesterday) Breast mesh products marketed as “internal bras” for lift and augmentation surgeries are now under investigation amid reports of painful complications, and questions over manufacturers’ prior knowledge of mesh-related risks. MORE ABOUT: BREAST MESH LAWSUITBreast Mesh Problems Prompted FDA Warnings Over Off-Label Use (10/15/2025)Breast Mesh Lawsuits May Follow Recent Studies Highlighting Internal Bra Complications (10/09/2025)FDA Warns BD Surgical Mesh Products Not Proven Safe for Breast Reconstruction Surgery (11/10/2023)
Four BioZorb Breast Marker Lawsuits Set for Trial Between Jan. and April 2026 (Posted: 4 days ago) A federal judge has set key scheduling deadlines for the four first bellwether trials over claims that BioZorb breast markers are defectively designed. MORE ABOUT: BIOZORB LAWSUITLawyers in BioZorb Implant Lawsuits Request Updated Deadlines in Pretrial Schedule (10/15/2025)Tamoxifen Side Effects Linked to Uterine Tumors in Breast Cancer Patients: Study (09/16/2025)Five Women File Joint Lawsuit Over BioZorb Breast Implant Side Effects (09/09/2025)
Lawsuits Over Depo-Provera and Meningioma To Be Coordinated Between Federal and State Courts (Posted: 5 days ago) Parties in federal Depo-Provera meningioma lawsuits seek closer coordination with Delaware and New York state courts, proposing a synchronization of general causation schedules. MORE ABOUT: DEPO-PROVERA LAWSUITDepo-Provera Side Effects Hidden for Decades, Lawsuit Alleges (10/20/2025)Over 1,300 Depo Shot Lawsuits Now Being Pursued by Women With Meningioma Tumors (10/06/2025)Depo-Provera Brain Tumor Lawsuit Describes Left-Sided Numbness, Tingling Before Diagnosis (10/01/2025)