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.
Ethicon Opposes Centralization of Hernia Physiomesh Lawsuits April 17, 2017 Austin Kirk Add Your Comments As the U.S. Judicial Panel on Multidistrict Litigation (JPML) considers whether to consolidate all hernia mesh lawsuits filed over problems with Ethicon Physiomesh, the manufacturer argues that the claims will be too individualized to warrant centralization before one judge for coordinated pretrial proceedings. Johnson & Johnson’s Ethicon subsidiary filed a response (PDF) last week, after a group of plaintiffs asked that all cases pending in U.S. District Courts nationwide be transferred to one judge to reduce duplicative discovery into common issues, avoid conflicting pretrial rulings and to serve the convenience of the parties, witnesses and the courts. There are currently several dozen Ethicon Physiomesh lawsuits pending throughout the federal court system, each involving similar allegations that problems with the design of the hernia patch caused individuals to suffer painful and debilitating complications, often resulting in the need for multiple surgical procedures to remove the mesh after it failed. 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 Ethicon Physiomesh is a type of hernia patch introduced in March 2010, which has been widely used during hernia repair surgery in recent years. However, the product has been plagued by reports of complications, including adhesions, perforations, infections, mesh erosion and the need for hernia revision surgery. After failing to identify the cause of these hernia repair complications, the manufacturer decided to remove the product from the market worldwide in May 2016. The Ethicon hernia mesh recall was classified as a “market withdrawal” in the United States, but all hospitals were asked to return unused implants and the manufacturer does not intend to return the product to the market. As a growing number of complaints continue to be filed by individuals nationwide, a group of plaintiffs filed a motion with the U.S. JPML in March, seek to centralize and coordinate the hernia Physiomesh lawsuits. In the response filed last week, the manufacturer attempts to argue that each of the cases will involve individualized facts, citing a wide range of different hernia mesh injuries reported among the plaintiffs. “Here, individualized issues for each plaintiff will eclipse any purported common ones, making an MDL ineffective at narrowing claims and issues,” the brief states. “Although Plaintiffs may point to hernia recurrence as the common injury that binds these cases together, a closer look at the complaints shows a wide variety of alleged injuries, such as abdominal abscesses and intestinal fistula, bowel puncture, erosion and bowel resection, bowel adhesions, fistula and infection, and recurrent inguinal hernia.” Ethicon also argues that the creation of a Physiomesh MDL will result in numerous lawsuits to be filed that have no merit, in an effort to force the company to reach a hernia mesh settlement. In complex product liability litigation, where a large number of separate claims are filed throughout the federal court system involving similar damages caused by a medical device or medication, it is common for the U.S. JPML to centralize the cases for discovery and bellwether trials. The U.S. JPML is scheduled to consider oral arguments on the motion during an upcoming session set for May 25, at the John H. Wood, Jr. U.S. Courthouse in San Antonio, Texas. Tags: Ethicon, Hernia, Hernia Mesh, Johnson & Johnson, Physiomesh 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 0 Comments 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: today) 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: 3 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: today) 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: 3 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: 4 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)