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.
Chlorpyrifos Parkinsonโs Disease Lawsuit Chlorpyrifos lawsuits are being investigated for individuals diagnosed with Parkinsonโs disease after direct, residential, occupational or Gulf War pesticide exposure.
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.
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.
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.
Zimmer Hip Problems Caused By M/L Taper System, Lawsuit Alleges November 7, 2018 Irvin Jackson Add Your CommentsA California man indicates that problems following a hip replacement were caused by defects with the Zimmer M/L Taper hip components used during his procedure, indicating that the cobalt-chromium femoral heads represent an unreasonable risk of harm to individuals who receive the implant.The complaint (PDF) was filed by Donald and Janis Fletcher in the U.S. District Court for the Eastern District of California on November 5, indicating that Zimmer Biomet Inc. sold hip components that were defectively designed.Fletcher received a Zimmer M/L Taper Hip System in his right hip in December 2007. However, the Zimmer hip caused problems to develop, which resulted in the need for revision surgery in September 2018.Stay Up-to-Date Abouthip replacement lawsuitsAboutLawsuits.com sends a weekly digest email with information about recalls, lawsuits and warnings that may impact your family, which will include any new hip replacement lawsuit updates or developments. "*" indicates required fieldsEmail* SIGN ME UPΔ Learn MoreStay Up-to-Date AboutHip Replacement LawsuitsAboutLawsuits.com sends a weekly digest email with information about recalls, lawsuits and warnings that may impact your family, which will include any new hip replacement lawsuit updates or developments."*" indicates required fieldsEmail* SIGN ME UPΔ Learn MoreThe lawsuit alleges that the Zimmer hip implant is prone to fretting and corrosion at the head-neck/stem taper junctions, resulting in the release of toxic metal debris, metal ions, and other toxic byproducts.“Defendants were aware of the problems when they designed, manufactured, marketed, distributed, and/or sold the Zimmer M/L Taper Hip System,” the lawsuit states. “Nonetheless, Defendants employed the design in its Zimmer M/L Taper Hip System in reckless disregard for the safety of patients, including Plaintiff.”The problems experienced by Fletcher are similar to the issues that gave rise to aย Stryker LFit v40 hip recallย in August 2016, according to the complaint. Fletcher indicates that both the LFit v40 femoral head and the Zimmer Versys femoral heads are made of cobalt-chromium, and both are typically mated with metal alloy stems that result in an increased risk of โtaper lock failureโ and excessive metal debris.Zimmer currently faces a growing number of similar complaints filed in recent months over the combination of the Zimmer M/L Taper Hip Prosthesis and Zimmer VerSys Hip femoral head, which are consolidated in the federal court system before U.S. District Judge Paul A Crotty in the Southern District of New York, as part of an MDL, or multidistrict litigation.More than 100,000 of these Zimmer hip replacements have been implanted throughout the United States, according to recently filed court documents. Asย lawyers continue to investigate and review potential casesย in the coming months and years, it is expected that the size of the litigation may increase rapidly. 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: Hip Replacement System, Metal-on-Metal Hip, Metallosis, Zimmer, Zimmer Hip ReplacementMore Hip Replacements Lawsuit Stories Hip Replacement Lawsuit Claims System Failure Caused Woman To Suffer โDusky Metal Diseaseโ June 5, 2026 Biomet Hip Lawsuit Filed Over Defective M2A Metal-on-Metal Implant December 26, 2024 Zimmer Biomet Lawsuit Filed Over RibFix Blu Implant Fracture September 25, 2024 2 Comments David May 31, 2025 Trying to find out what Zimmer products were installed in my left hip’s that Theodore September 25, 2019 I had a Zimmerman ml taper hip replacement in 2008 and I was told by the F.D.A that it was recalled I just seen the orthopedic surgeon who did the surgery and had did a x-ray and still didn’t let me know that the femoral head was recalled I developed hetrotopic ossification in my hip and alot of groin pain been going through this pain for a long time and the therapy doesn’t help and now since I was not putting pressure on my left hip my right hip needs a replacement I reported it all to the F.D.A and they asked me if the surgeon told me and I told them he did not tell me nothingLinkedInThis 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. 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