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.
Zimmer M/L Taper Hip System Released Toxic Levels Of Cobalt And Chromium: Lawsuit October 30, 2018 Irvin Jackson Add Your CommentsA North Carolina man indicates that problems with the Zimmer M/L Taper Hip System resulted in the release of toxic levels of cobalt and chromium into his blood, resulting in the loosening and failure of his hip replacement implant.ย Robert Fick filed a product liability complaint (PDF) against Zimmer, Inc. earlier this month in the U.S. District Court for the Middle District of North Carolina, indicating that the company sold a defective hip implant, which has been linked to a large number of reported problems.According to the lawsuit, Fick had a Zimmer M/L Taper Hip System implanted in February 2012, which included a Versys 12/14 Tapered Cobalt-Chromium (CoCr) femoral head.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 More“Despite [reassurances of device safety], the defective design and manufacture of the Zimmer M/L Taper Hip System, with a CoCr femoral head generates excessive fretting and corrosion occurring at the head-neck/stem taper junctions,” the complaint states. “The fretting and corrosion generates toxic metal debris, metal ions and other chemical byproducts which are released into the surrounding tissues. These metal debris, metal ions and byproducts destroy the surrounding tissue and bone, often causing pseudotumors, and other metal related conditions. The release of metal debris and metal ions also causes systemic exposure to toxic metallic elements, often reflected in elevated blood serum and/or urine testing levels.”After experiencing metallosis, pseudotumor and severe trunnionosis, Fick’s hip replacement failed, resulting in the need for revision surgery in March 2016.The problems experienced by Fick are similar to the issues that gave rise to a Stryker LFit v40 hip recall in August 2016, according to the complaint. Fick 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 “taper lock failure” 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.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.In August, a group of plaintiffs filed a motion toย centralize all Zimmer hip lawsuits over the VerSys, M/L Taper and M/L Taper with Kinective Technology, asking the U.S. Judicial Panel on Multidistrict Litigation (JPML) to transfer cases filed in various different federal district courts to U.S. District Judge Donovan Frank in Minnesota for coordinated discovery and pretrial proceedings. 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 Replacement, Zimmer VersysMore Hip Replacements Lawsuit Stories 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 Zimmer Biomet CPT Hip System Linked to Increased Risk of Thigh Bone Fractures, FDA Warns September 18, 2024 2 Comments Christine November 18, 2023 I had a Zimmer ML taper hip prosthesis surgery in 2005, Versys hip system with femoral head. I am suffering from metal ion debris accumulation in my groin and very high level of cobalt and chromium in my blood. Difficulty walking and climbing stairs. Pain in hip area. Gustavo September 29, 2021 I had a new hip in 2005(resurfacing) the prosthesis was faulty and in 2011 after 6 years in a lot of pain, I was in a class action and because I had a revision, I was awarded( for ruined my sport life) 39,000 canadian funds. My pain kept growing and they checked, they found high levels of chromium and also have a 7cm pseudo tumor. They said I have to get the metal app ASAP and I am having my third replacement next week October 5th 2021. I was also told that the cup was irritating the illio psoas and that was proven to be also the case after the injected cotisone snd was the first time since 2006 that I was almost s month without pain. Now of course is back. How is possible that they can go away with this? I was depressed already for16 years and nobody did anything for me. Any help would be appreciated. Gustavo Sedler 604 836-7460 Thank you fron Vancouver, Canada.CompanyThis 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 SmartPort Surgery Lawsuit Claims AngioDynamics Catheter Fractured Inside Womanโs Body (Posted: today)A Missouri woman alleges her AngioDynamics SmartPort catheter fractured and left a broken piece near her heart, requiring surgical removal after it was found during a CT scan.MORE ABOUT: ANGIODYNAMICS PORT CATHETER LAWSUIT18 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)Vortex Port Lawsuit Filed After Port Catheter Removed Due to Infection, Blood Clots (04/09/2026) Enfamil NEC Lawsuit Cleared For MDL Trial in July 2026 (Posted: yesterday)A federal judge has selected an Enfamil lawsuit to serve as the first NEC infant formula bellwether trial, which is set to begin in July.MORE ABOUT: ENFAMIL AND SIMILAC BABY FORMULA LAWSUITLawsuit Claims Cowโs Milk-Based Baby Formula Use Resulted in Infant Suffering Devastating NEC Symptoms (05/08/2026)Mead Johnson Lawsuit Claims Premature Child Developed NEC From Enfamil (04/24/2026)Similac NEC Lawsuit Payout Increased by $17M in Punitive Damages (04/14/2026) Abbott Eterna Lawsuit Alleges Spinal Cord Stimulator Malfunction Resulted in Worsening Pain (Posted: 2 days ago)According to a lawsuit brought against the manufacturer and the FDA, an Abbott Eterna spinal cord stimulator has caused pain, shocks and complications instead of the relief promised.MORE ABOUT: SPINAL CORD STIMULATOR LAWSUITNevro Stimulator Lawsuit Alleges SCS Lead Failure Caused Nerve Damage (05/06/2026)Lawsuit Claims Abbott, Boston Scientific SCS Pre-Market Approval Supplements Caused Permanent Injuries (04/29/2026)JPML Sets Hearing Over Spinal Cord Stimulator Lawsuit Consolidation for May 28 (04/24/2026)
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