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.
Stryker Accolade, LFit V40 Hip Components Caused Pseudotumor, Metallosis: Lawsuit March 16, 2017 Irvin Jackson Add Your CommentsA product liability lawsuit filed by a Texas woman alleges that recalled Stryker Accolade and LFit v40 hip components caused her to develop metal blood poisoning and pseudotumors, which resulted in severe pain and the need for revision surgery only a few years after her original hip replacement.ย The complaint (PDF) was filed by Betty Sadler in the U.S. District Court for the Southern District of Texas on March 7, against Howmedica Osteonics Corp., which does business as Stryker Orthopedics.Sadler indicates that she underwent a total hip arthroplasty in October 2008, at which time a Stryker Accolade TMZF Plus femoral stem and LFit V40 femoral head has implanted due to left hip degenerative arthrosis.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“Approximately seven years after her total hip arthroplasty, Plaintiff began experiencing significant left hip pain and discomfort,” the lawsuit states. “Upon MRI evaluation, a left hip pseudotumor was discovered.”When Sadler underwent hip revision surgery in January 2016, surgeons discovered not only the pseudotumor, but also evidence of metallosis, which is a form of blood poisoning caused by metal debris, trunnionosis, and osteolysis. Surgeons replaced the cobalt chrome head of the LFit V40 with one made of ceramic due to the complications.After receiving similar reports of problems, a Stryker LFit v40 hip recall was issued last summer by the manufacturer, impacting certain large-diameter femoral heads sold before 2011. At that time, Stryker acknowledged that a higher-then-expected number of individuals were experiencing problems with trunnion failure, metal wear, adverse tissue reactions and other complications.The case filed by Sadler now joins a growing number of other Stryker Accolade hip lawsuits filed in recent months over problems when the femoral head was combined with this Stryker hip stem.As hip replacement lawyers continue to review cases for individuals who are just now learning that complications experienced in recent years may have been caused by design problems, it is expected that several thousand lawsuits may be filed in the coming months and years. 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 Implant, Howmedica, Metallosis, Stryker, Stryker Accolade, Stryker LFit Image Credit: |More 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 0 CommentsPhoneThis 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 Suboxone Manufacturer Faces Nearly 18,000 Dental Erosion Lawsuits (Posted: today)Indivior faces nearly 18,000 Suboxone dental erosion lawsuits filed by individuals nationwide who say the opioid addiction treatment caused severe tooth damage.MORE ABOUT: SUBOXONE TOOTH DECAY LAWSUITSuboxone Dry Mouth Lawsuit Claims Dental Problems Could Have Been Avoided With Sublocade Shot (06/18/2026)Suboxone Dental Erosion Lawsuit Alleges Indivior Should Have Known About Tooth Decay Risks (06/11/2026)Suboxone Oral Film Lawsuit Claims Opioid Treatment Causes Tooth Decay (05/20/2026) Nevro SCS Lawsuits Warrant Centralization in New MDL: Motion (Posted: yesterday)Plaintiffs have requested that the Judicial Panel on Multidistrict Litigation consolidate all Nevro spinal cord stimulator lawsuits in the Central District of California for pretrial procedures.MORE ABOUT: SPINAL CORD STIMULATOR LAWSUITProclaim Spinal Cord Stimulator Lawsuit Follows Infection, Battery Migration Problems (07/06/2026)MDL Sought for Abbott Spinal Cord Stimulator Lawsuits (06/29/2026)Lawsuit Alleges WaveWriter Alpha Spinal Cord Stimulator Problems Caused Burning, Shocking Sensations (06/24/2026) Vortex Port Lawsuit Claims Defective AngioDynamics Device Caused Infection, Pulmonary Embolism (Posted: 2 days ago)An AngioDynamics Vortex port lawsuit alleges the implantable port catheter caused a South Carolina woman to suffer pulmonary embolisms and a serious infection requiring surgical removal.MORE ABOUT: ANGIODYNAMICS PORT CATHETER LAWSUITAngioDynamics Port Catheter Lawsuit Claims Womanโs SmartPort Implants Caused Multiple Infections (06/23/2026)Xcela Port Lawsuit Claims AngioDynamics Catheter Caused Thrombosis (06/12/2026)Port Catheter Thrombosis Lawsuit Claims Defective AngioDynamics Xcela Device Caused Injury (06/03/2026)
Hip Replacement Lawsuit Claims System Failure Caused Woman To Suffer โDusky Metal Diseaseโ June 5, 2026
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