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.
Exactech Optetrak Logic Knee Removed Due to Tibial Insert “Fraying”, Lawsuit Alleges Knee replacement tibial insert degraded and released plastic pieces into the body over first four years it was implanted, leading to failure of the knee replacement and need for revision surgery July 18, 2022 Irvin Jackson Add Your Comments Although knee replacements are expected to last about twenty years, a New York man indicates in a recently filed lawsuit that an Exactech Optetrak Logic tibial insert severely degraded and released polyethylene plastic pieces into the surrounding tissue, resulting in the need for knee revision surgery only four years after the implant was placed in his body. The complaint (PDF) was filed by Christopher Matchett and his wife, Rebecca, in the U.S. District Court for the Southern District of New York on July 9, indicating that the tibial insert “fraying” was caused by a packaging defect, which impacted thousands of Exactech knee replacement components distributed since 2004 An Exactech knee recall was issued in February 2022, after the manufacturer acknowledged that “out-of-specification” vacuum bags were used with more than 140,000 polyethylene inserts included with Optetrak, Optetrak Logic and Truliant total knee replacement systems, which exposed the plastic tibial inserts to oxygen before they were implanted. The Machetts now joins a growing number of families pursuing Exactech knee replacement lawsuits, alleging that their lives have been negatively effected when the implants failed prematurely, resulting in severe and permanent injuries. Learn More About Knee Replacement Lawsuits If you or a loved one experienced complications or required revision surgery due to a defective knee replacement implant, you may be entitled to financial compensation. Learn More SEE IF YOU QUALIFY FOR COMPENSATION Learn More About Knee Replacement Lawsuits If you or a loved one experienced complications or required revision surgery due to a defective knee replacement implant, you may be entitled to financial compensation. Learn More SEE IF YOU QUALIFY FOR COMPENSATION The lawsuit indicates Christopher Matchett had an Exactech Optetrak Logic Total Knee System implanted in his left knee in January 2014, but he began to experience problems within only a few years. “A 2018 MRI showed that Plaintiff was suffering from debris synovitis due to fraying of the original implant’s plastic components, namely the tibial insert,” the lawsuit states. “Not only had the original implant failed very prematurely, but upon explantation, it was confirmed that the implant’s polyethylene components had severely degraded, releasing pieces of polyethylene plastic into his knee cavity and surrounding tissues, and thus triggering inflammation and other phenomenon associated with an immune response in and around the Plaintiff’s knee. Matchett had the implant removed in April 2018, resulting in it being replaced with yet another Optetrak Logic knee system. However, the second implant failed as well, according to the results of an MRI performed in May 2022, causing even more damage to the plaintiff’s knee cavity and surrounding tissue. Exactech Knee Replacement Problems Reported Years Before Recall Years before Machett had the Exactech knee implant placed in his body, the manufacturer was receiving reports of similar problems with the tibial inserts and premature revision rates among patients. As early as 2017, lawsuits over Exactech knee implants indicated there were alarming rates of adverse event reports being submitted to the FDA involving premature knee replacement revision surgery, which resulted in what some said was a “silent” Exactech recall when the company began slowly and quietly replacing the tibial trays of some Optetrak models. In the recall notice issued earlier this year, the manufacturer now acknowledges the foreign registries have found a higher-than-expected rate of Exactech knee revision surgery caused by a degraded poly liner. As individuals continue to experience problems and require Exactech knee replacement revision surgery in the future, it is expected that thousands of similar lawsuits will be filed throughout the U.S. Court system. Tags: Exactech, Knee Implant, Knee Implant Recall, Knee Replacement System, Optetrak More Knee Replacement Lawsuit Stories Zimmer Biomet Bone Cement Lawsuit Filed Over Failed Knee Replacement July 10, 2025 Biomet Signature Vanguard Knee Replacement Lawsuit Alleges Pegs in Regenerex Patella Sheared, Broke May 13, 2025 Exactech Recall Lawsuits Placed On Hold While Bankruptcy Process Plays Out November 11, 2024 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 TermPhoneThis 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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