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.
Hernia Mesh Bowel Adhesions Result in Lawsuit Over Ethicon Physiomesh May 1, 2017 Irvin Jackson Add Your Comments Due to problems with the Ethicon Physiomesh used during ventral hernia repair, a Delaware man indicates that he suffered a number of small bowel adhesions, resulting in the need for the surgical mesh to be removed from his body. The complaint (PDF) was filed by Charles Racine on April 13, indicating that Johnson & Johnson and its Ethicon sold a hernia mesh product with numerous defects, which created a high risk of unreasonable and dangerous injuries, which may result in severe and permanent health consequences. Racine had an Ethicon Physiomesh patch implanted in March 2014, during surgical repair of a ventral hernia. However, just a week later he returned to the hospital, suffering abdominal pain, vomiting and diarrhea. 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 It was not until February 2016 that doctors were able to diagnose his health problems, finding that he suffered significant adhesions in his abdomen, with loops of small bowel attached to the mesh and adhesions in the upper and mid abdomen. “Mr. Racine’s severe adverse reaction, and the necessity for further surgical removal of the Physiomesh, directly and proximately resulted from the defective and dangerous condition of the product and Defendants’ defective and inadequate warnings about the risks associated with the product, and the frequency, severity and duration of such risks,” the lawsuit states. “The Physiomesh implanted in Mr. Racine failed to reasonably perform as intended. The mesh caused serious injury and will require additional invasive surgery to properly fully remedy.” Racine points to numerous design defects, indicating that the material used in Ethicon Physiomesh is not inert and therefore reacts to human tissue, and harbors infections. The hernia mesh components are also prone to migrate from the implant location, according to the lawsuit, which claims that the hernia mesh regularly fails and requires removal that causes damage to organs and tissue. The case joins a growing number of Ethicon Physiomesh lawsuits filed in recent months over hernia mesh bowel adhesions and other complications, each raising similar allegations that the manufacturer knew or should have known about the risk of problems. However, rather than promptly issuing a nationwide hernia mesh recall, the manufacturer opted to simply remove the product from shelves and cease further sales within the United States last year. As hernia mesh lawyers continue to review and file a number of lawsuits for individuals nationwide who had Ethicon Physiomesh implanted, a motion was filed last month with U.S. Judicial Panel on Multidistrict Litigation (JPML), seeking to transfer all cases to the Middle District of Florida for coordinated discovery pretrial proceedings. The panel will consider oral arguments on the motion during an upcoming hearing session scheduled for May 25, in San Antonio, Texas. 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 1 Comments Susan May 3, 2017 I 1st had it put in 2012 in belacel area then 6 months later got a spangle on left side 1013 died on table Dr brought me back. I asked and they said it is too dangerous to be removed. May 1,2017 was when i got resp back from my dr. May 9th im going in too have test done and also mri or what they need to do too find out why my stomic hurts so much. Can not have jeans over stomic area and also sleeping on left or right side is ouch but when i take sleeping pills for nerve nerothey then i am out and don’t know much till im awake again. And can not sleep on my stomic. My sugerie papers state i have the mash in both areas. And both were hernia repairs. They also said they were going to poss do blood work as well. But since it can not be removed know what? Pain for life? God i hope not. 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 TermEmailThis 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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