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.
Hernia Mesh Trial Involving Ethicon Physiomesh Set To Begin June 22, 2020 September 27, 2019 Irvin Jackson Add Your Comments The U.S. District Judge presiding over all federal Ethicon Physiomesh lawsuits has indicates that the first federal “bellwether” trial will begin on June 22, pushing back the pretrial schedule about two months. Ethicon Physiomesh is a multi-layered, flexible composite hernia mesh product introduced by Johnson & Johnsonโs Ethicon subsidiary in 2010. However, the manufacturer removed the product from the market only six years later, amid a large number of complaints involvingย complications with the hernia mesh, often resulting in the need for additional surgery to remove it from individualsโ bodies. There are currently more than 2,300 product liability lawsuits over Ethicon Physiomesh pending throughout the federal court system, each raising similar allegations that the manufacturer sold a defective and unreasonably dangerous product, which caused plaintiffs to suffer severe abdominal pain, infection, hernia recurrence, adhesions, perforations, erosion and other injuries associated with a hernia mesh failure. 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, the federal cases is centralized for pretrial proceedings before U.S. District Judge Richard Story in the Northern District of Georgia, as part of an MDL, or multidistrict litigation. To reduce duplicative discovery into common issues in the cases, avoid conflicting rulings from different courts and to serve the convenience of parties, witnesses and the judicial system, cases filed in U.S. District Courts nationwide are consolidated before Judge Story for coordinated discovery and a series of early โbellwetherโ trials, which will test the relative strengths and weaknesses of the cases. In June, Judge Story announced that the first bellwether trial would go before a federal jury on April 20, 2020. However, in an amended practice and procedure order (PDF) issued on September 23, the start of the first hernia mesh trial in the litigation has been pushed back to June 22, 2020. The order indicates that by January 27, 2020, the Court will decide the manner of trial, the order of selection for plaintiffs and the timing of additional trial cases. Daubert motions challenging the admissibility of expert witness testimony will be due in each trial case by February 24, 2020, and the Court indicates that a pre-trial conference will be set at an appropriate time before the first trial begins in June. While the outcomes of this hernia mesh trial, and any other early bellwether cases that go before a jury, will not be binding on other plaintiffs, it will be closely watched by lawyers involved in the litigation and may greatly influence any eventuallyย hernia mesh settlementsย that may be necessary for Ethicon to avoid thousands of individual trial dates nationwide. In addition to lawsuits over problems with Ethicon Physiomesh, a number of similar claims are being pursued against manufacturers of other polypropylene products introduced in recent years, including Bard hernia mesh, Covidien Parietex mesh, Atrium C-Qur and other products. 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: Ethicon, Hernia, Hernia Mesh, Johnson & Johnson, Physiomesh 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 1 Comments Joan March 4, 2020 I just donโt understand why the court continues over and over to keep pushing the 1st bellwether Ethicon hernia cases. It literally blows my mind that the companies being sued SPEND millions and millions of dollars to continue slowing the process down. They pay that money to their attorneys, again millions. Instead of trying to get these cases heard sooner, saving much of those millions, and paying instead to the actual people that were injured due to their product. Also MDL suits are supposed to speed up the process yet everything Iโve read takes so much longer for the individual than had they just found an attorney to keep there case as an individual suit. I also think that plaintiffโs should be given notice that their cases are being directed to the MDL suit, they should be contacted and be allowed to make the decision. InstagramThis 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. 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