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.
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.
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.
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.
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.
Change Healthcare Lawsuit Lawyers are reviewing Change Healthcare class action lawsuits for individuals who had their personal information stolen due to the data breach.
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.
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.
Processed Food Lawsuit Lawsuits are being pursued against the food industry over their manufacturing and advertising of ultra-processed foods, which have caused a generation of children to face an increased risk of developing childhood diabetes and other chronic illnesses.
Short Form Hernia Mesh Complaint Approved for Ethicon Physiomesh Cases September 25, 2017 Austin Kirk Add Your Comments The U.S. District judge presiding over all federal Ethicon Physiomesh lawsuits has approved a Short Form Complaint, which will be used to file all future hernia mesh complaints on behalf of individuals who have experienced problems, and provide a uniform method of describing the allegations for each case. Since June 2017, all federal product liability lawsuits over problems with Ethicon Physiomesh have been centralized before U.S. District Judge Richard Story in the Northern District of Georgia, to reduce duplicative discovery into common issues in the cases, avoid conflicting rulings from different courts on pretrial matters and to serve the convenience of the parties, witnesses and the judicial system. Each of the hernia mesh lawsuits involve similar allegations that Ethicon Physiomesh was defectively designed and manufactured, and that Johnson & Johnson and its Ethicon subsidiary failed to adequately warn patients and the medical community of the risks of complications, including adhesions, infections and the need for revision surgery. 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 a Practice and Procedure Order (PDF) issued on September 20, Judge Story approved a Short Form Complaint to be used when filing all future cases, outlining which allegations from a Master Complaint are being adopted by each plaintiff, and providing specific information about when and where the mesh was implanted. All pending cases will also be required to file a Short Form Complaint, which is designed to standardize the gathering of information about hundreds of potential cases that may be filed against Ethicon directly in the federal multidistrict litigation (MDL). While there are currently only about 116 Ethicon Physiomesh complaints pending the federal court system, as lawyers continue to review potential claims for individuals who have experienced complications following hernia repair, it is ultimately expected that several thousand lawsuits will be filed in the Ethicon Physiomesh MDL. Johnson & Johnson’s Ethicon unit introduced Physiomesh in March 2010, containing an absorbable film coating on each side of a polypropylene hernia mesh, which was designed to help the patch incorporate into the body and minimize inflammation. However, the hernia mesh was recalled last year, after a higher-than-expected number of individuals required revision surgery due to problems with the design. As part of the coordinated MDL proceedings, it is expected that a small group of Ethicon Physiomesh cases will be selected for a “bellwether” process, which is designed to help the parties gauge relative strengths and weaknesses of their claims. Through a unified short-form complaint, parties are able better able to identify representative cases. Following any bellwether trials in the MDL, if the parties fail to reach hernia mesh settlements for individuals who had an Ethicon Physiomesh patch fail, each individual complaint may be transferred back to the U.S. District Court where it originally would have been filed for a future trial date. Tags: Ethicon, Hernia, Hernia Mesh, Johnson & Johnson, Physiomesh More Hernia Mesh Lawsuit Stories Covidien Parietex Optimized Composite (PCOx) Hernia Mesh Lawsuits To Be Prepared for Trial May 21, 2025 Second Bellwether Trial in Covidien Hernia Mesh Lawsuit MDL Set for July 2026 May 14, 2025 Covidien Mesh Lawsuit Set For Trial in Feb. 2026, Over Defective Hernia Implant April 10, 2025 0 Comments 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 TermCommentsThis field is for validation purposes and should be left unchanged. Δ MORE TOP STORIES Depo-Provera Shots Triple Brain Tumor Risks Compared to Birth Control Pill: Study (Posted: today) Canadian researchers say receiving Depo-Provera injections for more than a year triples the risk of brain tumors compared to women who take birth control pills. 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Covidien Parietex Optimized Composite (PCOx) Hernia Mesh Lawsuits To Be Prepared for Trial May 21, 2025
Depo-Provera Shots Triple Brain Tumor Risks Compared to Birth Control Pill: Study (Posted: today) Canadian researchers say receiving Depo-Provera injections for more than a year triples the risk of brain tumors compared to women who take birth control pills. MORE ABOUT: DEPO-PROVERA LAWSUITDepo-Provera Lawsuit Pre-Settlement Funding and Loans Must Be Disclosed Under Court Order (07/09/2025)Depo-Provera Wrongful Death Lawsuit Blames Injections for Fatal Brain Tumor (07/02/2025)Lawsuit Alleges Depo-Provera DMPA Injection Increases Brain Tumor Risks (06/20/2025)
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