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.
Five Different Bard and Ethicon Hernia Mesh Patches Failed Over Less Than A Decade, Lawsuit Alleges August 1, 2019 Irvin Jackson Add Your Comments Following multiple hernia repair procedures, a Georgia man has filed a product liability lawsuit that indicates at least five different types of Bard and Ethicon hernia mesh failed, resulting in numerous health problems and injuries. The complaint (PDF) was filed by Ralph Miller in the U.S. District Court for the District of Rhode Island on July 17, indicating that design problems with Ethicon Proceed, Ethicon Physiomesh and three different Bard Ventralight patches caused a series of complications he experienced over a period of about ten years. Miller’s problems started in January 2010, when surgeons implanted him with an Ethicon Proceed Surgical Mesh to repair a ventral hernia. However, by December of that year, he required revision surgery due to a hernia mesh failure, which caused him to suffer dense adhesions. 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 In December 2010, the Proceed patch was removed, and surgeons implanted Ethicon Physiomesh, which was later reported amid reports of problems linked to the multi-layered polypropylene mesh design. Miller indicates that he also experienced complications when the Ethicon Physiomesh failed, resulting in large adhesions and the need to remove the patch in November 2012. At that time, Miller was implanted with three Ventralight ST mesh patches, manufactured by C.R. Bard. However, in June 2019 he was diagnosed with chromic wall and groin pain linked to those meshes and was placed on short-term disability. “Defendants were fully aware of the dangers defective products they were placing into the stream of commerce posed to their customers, specifically the Mesh Products polypropylene mesh, which has been shown to pose an unreasonable risk of human body inflammation, granuloma formation, foreign body reaction, excessive scar tissue formation and long-term complications,” the lawsuit states. “Despite the abundance of scientific and medical information available relating to the dangerous properties and serious risks of the Mesh Products, Defendants deliberately ignored these dangers and aggressively promoted the Mesh Products polypropylene mesh to healthcare providers and/or directly to consumers.” The complaint raises allegations that are similar to those presented in other hernia mesh lawsuits filed in recent months against Ethicon and Bard over similar polypropylene hernia patch designs used in thousands of procedures nationwide. Several thousand Ethicon Physiomesh lawsuits have been filed over complications with this recalled product, which was removed from the market in 2016 amid a large number of reports involving premature failure. Similar allegations have also been raised in other Bard hernia mesh lawsuits, involving complications linked to Ventralight and other polypropylene mesh. Each of the complaints involve similar allegations, indicating that hernia mesh implants used in recent years were defectively designed, unreasonably dangerous, and prone to failure, migration, and infections, often resulting in recurrent hernias and the need for revision surgery. 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: Bard, C. R. Bard, Ethicon, Ethicon Proceed Mesh, Hernia, Hernia Mesh, Johnson & Johnson, Physiomesh, Ventralight 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 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 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)
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)