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.
Atrium C-Qur Hernia Mesh Cases Selected for Initial Bellwether Trial Pool August 14, 2018 Austin Kirk Add Your Comments With hundreds of Atrium C-Qur lawsuits pending in the federal court system, each involving similar allegations that individual suffered painful complications from the hernia mesh, a group of 16 cases have been selected for an initial discovery pool, which will be eligible for early trial dates in the litigation. Atrium C-Qur (pronounced โsecureโ) was a widely used hernia repair product, which was introduced in March 2006, featuring a unique design that involved a polypropylene mesh with an Omega-3 fatty acid (O3FA) gel coating. While this was designed to reduce scar tissue formation, while promoting fixation of the mesh to the abdominal wall, the C-Qur patch has been linked to a large number of reported problems, including inflammatory responses, bowel adhesions and other painful complications. Nearly 500ย product liability complaints have been filed in the federal court system over problems with Atrium C-Qur mesh, claiming that the manufacturer sold an unreasonably dangerous and defective hernia repair system, which often results in the need for additional complex procedures to remove the patch months or even years after it is implanted. 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 Given similar questions of fact and law raised in the complaints, the U.S. Judicial Panel on Multidistrict Litigation (JPML) establishedย consolidated pretrial proceedings for all Atrium C-Qur hernia mesh casesย in December 2016, centralizing all claims before U.S. District Judge Landya McCafferty in the District of New Hampshire to reduce duplicative discovery into common issues, avoid conflicting pretrial rulings and to serve the convenience of the parties, witnesses and the judicial system. In a joint notice (PDF) filed on August 9, plaintiffs and defendants identified a group of 16 cases that have been selected for the initial bellwether pool. This group will subsequently be narrowed down to a smaller group of representative cases, which will be eligible for the first Atrium C-Qur trial date, scheduled to begin in February 2020. Following initial discovery in these cases, the group will be pared down to eight claims by March 1, 2019, with Plaintiffs selecting four and Defendants selecting four, which will continue with case-specific discovery and expert discovery, which is to be completed by September 20, 2019. Daubert motions on challenges to the admissibility of expert testimony will be filed by October 18, 2019, and responses are due by November 1, 2019, according to the order, which indicates that the first โbellwetherโ trial will begin on February 19, 2020. As part of the coordinated MDL proceedings before Judge McCafferty, the parties are scheduled to meet for a status conference on Thursday. According to joint agenda (PDF) submitted late last week, the parties also intend to address with the court a recently filed motion to extend jurisdictional discovery and briefing deadlines. While the outcomes of these โbellwetherโ trials will not be binding on other claims, the process is designed to facilitate potentialย hernia mesh settlementsย that may be necessary to avoid the need for hundreds of individual trials in various U.S. District Courts nationwide following the coordinated MDL proceedings. Tags: Atrium C-Qur, Atrium Medical, Hernia, Hernia Mesh Image Credit: | More Hernia Mesh Lawsuit Stories 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 Covidien Symbotex Mesh Lawsuit Reset For Trial in July 2026 November 24, 2025 0 Comments X/TwitterThis 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 Abbott Spinal Cord Stimulator Lawsuit Alleges Defects Caused Lead Migration, Electric Shocks (Posted: today) An Abbott spinal cord stimulator lawsuit filed by three women says the product was defectively designed, inappropriately approved by the FDA, and left them with severe injuries, worsening pain and the need for removal surgery. MORE ABOUT: SPINAL CORD STIMULATOR LAWSUITLawsuit Claims Airport Body Scanner Destroyed Woman’s Spinal Cord Stimulator, Requiring Surgical Removal (03/03/2026)Medtronic Spinal Cord Stimulator Lawsuit Filed Over Unnecessary Shocking Sensations (02/27/2026)Boston Scientific Pacemaker Lawsuit Claims Recalled Device Caused Life-Threatening Situation (02/25/2026) Dupixent Mycosis Fungoides Lawsuit Filed Over Failure To Warn About T-Cell Lymphoma Risks (Posted: yesterday) A Georgia couple’s lawsuit claims the makers of Dupixent failed to provide adequate warnings about the risk of mycosis fungoides, a type of T-cell lymphoma. 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Abbott Spinal Cord Stimulator Lawsuit Alleges Defects Caused Lead Migration, Electric Shocks (Posted: today) An Abbott spinal cord stimulator lawsuit filed by three women says the product was defectively designed, inappropriately approved by the FDA, and left them with severe injuries, worsening pain and the need for removal surgery. MORE ABOUT: SPINAL CORD STIMULATOR LAWSUITLawsuit Claims Airport Body Scanner Destroyed Woman’s Spinal Cord Stimulator, Requiring Surgical Removal (03/03/2026)Medtronic Spinal Cord Stimulator Lawsuit Filed Over Unnecessary Shocking Sensations (02/27/2026)Boston Scientific Pacemaker Lawsuit Claims Recalled Device Caused Life-Threatening Situation (02/25/2026)
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