Scope Infection Lawsuit Patients across the United States have filed medical scope infection lawsuits after contaminated endoscopes and duodenoscopes allegedly transmitted dangerous bacterial infections during procedures such as ERCP, colonoscopy, and other endoscopic treatments.
Spinal Cord Stimulator Lawsuit Spinal cord stimulator lawsuits allege that implanted pain devices malfunctioned, migrated, or caused nerve damage, often forcing patients to undergo revision or removal surgery.
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.
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.
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
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.
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.
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.
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.
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.
Knee Implant Failure Risks Increased By Bone Loss, Obesity, Unusual Bone Shape: Study February 16, 2018 Irvin Jackson Add Your CommentsResearchers from the OrthoCarolina Hip & Knee Center have identified several patient factors, which may contribute to the risk of knee implant failure following joint replacement surgery.ย In a study published in January edition of The Journal of Arthroplasty, researchers indicate that obesity, abnormal bone shapes, and bone loss all play a role factoring into catastrophic knee implant failures and the need for revision surgery.The research looked at data on 1,106 total knee arthroplasty (TKA) revision surgeries performed from 2004 to 2017, focusing on radiographic analysis of 27 cases that were performed at their institution.Learn More AboutKnee Replacement LawsuitsIf 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 MoreSEE IF YOU QUALIFY FOR COMPENSATIONLearn More AboutKnee Replacement LawsuitsIf 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 MoreSEE IF YOU QUALIFY FOR COMPENSATIONAccording to their findings, 26 out of the 27 patients had preoperative bone deformities. The average body mass index of those patients was 38, which is considered severely obese, and 25 out of the 27 had radiographic medial tibial bone loss prior to the implant collapsing.Researchers noted that as the average body mass index (BMI) in the U.S. has risen, so has the BMI of patients undergoing primary total knee arthroplasty. They noted that multiple studies have found that obesity increases the rate of knee implant complications. Previous studies have also pointed to increasing rates of mechanical failure of knee implants.“Obesity has been demonstrated to double the risk of aseptic tibial loosening in primary TKA,” the researchers noted. “It appears that increased tibial stress is a primary factor for this mode of failure.”The findings suggested that larger patients may require additional tibial fixation, and that it may surgeons should consider using selective criteria for increased tibial implant fixation to avoid problems. They recommended surgeons use three combined criteria: preoperative varus deformity in patients with a BMI of 35 or higher who require tibial components that are smaller than 50% of implant sizes.The findings come amid a growing number ofย knee replacement lawsuitsย filed in recent months over problems associated with several different types of systems widely used in recent years, which have been linked to high rates of implant failure, resulting in the need for knee revision surgery; includingย DePuy Attune Knee lawsuits,Exactech Optetrak Knee lawsuits, andย Arthrex iBalance knee lawsuits. Many of the problems with these implants have been linked to tibial loosening and tibial baseplate failures. Written by: Irvin JacksonSenior Legal Journalist & Contributing EditorIrvin 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: Arthrex, DePuy Attune Knee, Knee Implant, Knee Replacement, Obesity, OptetrakMore Knee Replacement Lawsuit Stories Exactech Implant Settlement Results in $8M Payout Over High Failure Rates September 19, 2025 Settlement Reached in Biomet Vanguard Knee Replacement Lawsuit August 14, 2025 Zimmer Biomet Bone Cement Lawsuit Filed Over Failed Knee Replacement July 10, 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 NoPost Comment I authorize the above comments be posted on this pageWeekly 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 TermΔ MORE TOP STORIES Depo-Provera Meningioma Side Effects Left Woman With Debilitating Migraines, Lawsuit Claims (Posted: yesterday)A Depo-Provera meningioma lawsuit indicates that a woman suffered permanent and debilitating injuries after needing to have a brain tumor surgically removed.MORE ABOUT: DEPO-PROVERA LAWSUITDepo-Provera Caused Meningioma 29 Years After First Birth Control Shots: Lawsuit (05/22/2026)Depo-Provera Lawsuit Filings Exceed 6,000, As Court Prepares for First Test Trials (05/18/2026)Intracranial Meningioma from Depo-Provera Shots Caused Hearing Loss, Vision Loss: Lawsuit (05/12/2026) Dupixent Injection Lawsuit Alleges Manufacturer Failed to Warn About T-Cell Lymphoma Cancer Side Effects (Posted: 2 days ago)Regeneron and Sanofi-Aventis face a Dupixent injection lawsuit from a Louisiana woman who says the companies knew about the drug’s risks but downplayed them to doctors and patients.MORE ABOUT: DUPIXENT LAWSUITDupixent Cancer Lawsuit Claims Eczema Drug Caused Womanโs CTCL Diagnosis (05/28/2026)Link Between Dupixent and Cancer Withheld From Doctors and Users, Lawsuit Alleges (05/11/2026)Lawsuit Indicates Dupixent Lymphoma Diagnosis Resulted in Multiple Rounds of Chemotherapy (05/01/2026) Port Catheter Thrombosis Lawsuit Claims Defective AngioDynamics Xcela Device Caused Injury (Posted: 3 days ago)A Nevada woman has filed a lawsuit alleging defects in AngioDynamicsโ port catheters caused her Xcela device to trigger a thrombosis in her right internal jugular vein.MORE ABOUT: ANGIODYNAMICS PORT CATHETER LAWSUITSmartPort Surgery Lawsuit Claims AngioDynamics Catheter Fractured Inside Womanโs Body (05/15/2026)18 AngioDynamics Port Catheter Lawsuits Will Be Selected for Bellwether Discovery in August 2026 (05/05/2026)AngioDynamics Catheter Lawsuit Claims SmartPort Device Embedded in Jugular Vein, Caused Embolism (04/30/2026)
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