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.
Wright Profemur Hip Settlement Reached to Avoid Trial December 12, 2013 Irvin Jackson Add Your CommentsWright Medical has agreed to settle a hip replacement lawsuit over problems with their Profemur modular stem, resolving the case shortly before trial was scheduled to begin.The settlement was reached in a Wright Profemur lawsuit filed by Timothy R. Courson and his wife, Linda Courson, which was expected to go to trial last month in the U.S. District Court for the Middle District of Georgia.About five days before trial was to begin, a settlement order (PDF) was entered by the Court, indicating that the parties reached an agreement to resolve the case. Terms of the settlement were not disclosed.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 case stems from a product liability complaint (PDF) filed by the Coursons in May 2012, which alleged that Timothy Courson received a hip replacement that included a Wright Profemur Plasma Z hip stem. In June 2011, the hip replacement failed and broke while Courson was walking at work, resulting in the need for revision surgery.Litigation Over Wright Profemur FracturesThe case is one of a number of Wright Profemur hip replacement lawsuits pending in courts throughout the country, which involve similar allegations that patients experienced problems when the modular femoral stem broke within a few years after implant.Unlike traditional hip replacement systems, which feature a single femoral component, the Wright Profemur stem features two modular pieces that allow the implant to be adjusted for leg length. However, plaintiffs claim that the design is prone to fret, corrode and ultimately fracture at the femoral neck stem.Courson alleged not only that the Wright Profemur hip was defective, but that the manufacturer sent a representative after his implant broke, who provided an extraction device that was supposed to aid in the revision surgery. However, Wright’s extraction device also broke while it was being used, causing Courson to suffer further damage and his physician had to perform another procedure to remove the Wright Medical Profemur and the company’s broken extraction device.Trial in the Courson case was being closely watched by product liability lawyers involved in the litigation, as it was expected to help gauge how juries may respond to evidence and testimony that may be similar to what will be offered throughout other cases.This is at least the second Wright Profemur hip settlement reached just before trial was set to begin. In April, aย settlement was reached in a Wright Profemur lawsuit filed by Gregory Tucker, with the agreement coming just a day after a judge denied an attempt by the manufacturer to have the case dismissed.Similar Lawsuits Over Stryker Rejuvenate Hip StemsThe allegations raised in the Wright Profemur litigation are similar to those made in Stryker Rejuvenate lawsuits, which involve a similar modular design.In July 2012, a Stryker Rejuvenate recall was issued amid reports that the the modular femoral neck-stem may corrode and fret, causing the implant to loosen and ultimately fail within a few years. An estimated 20,000 Stryker Rejuvenate or ABG II hip systems were sold in the United State before it was removed from the market, and nearly 1,000 complaints have already been filed in state and federal courts nationwide.Due to large scope of the Stryker Rejuvenate litigation, the U.S. Judicial Panel on Multidistrict Litigation (JPML) established coordinated proceeding in the federal court system in June 2013. All complaints filed in U.S. District Courts nationwide have been centralized in the District of Minnesota before U.S. District Judge Donovan Frank, as part of an MDL or Multi-District Litigation.In both the state and federal litigation, it is expected that a small group of Stryker Rejuvenate cases will be prepared for early trial dates, known as โbellwetherโ cases. These trials are designed to help the parties gauge how juries may respond to certain evidence and testimony that may be repeated throughout a large number of claims.The preparation and outcome of these bellwether trials may facilitate further negotiations toย settle Stryker Rejuvenate casesย without the need for individual trials in each lawsuit. 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, Stryker, Stryker ABG II, Stryker Rejuvenate, Wright Medical, Wright ProfemurMore 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 CommentsURLThis 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 Boston Scientific Spinal Cord Stimulator Lead Recall Issued After More Than 1,000 Serious Injuries (Posted: today)Certain Infinion CX spinal cord stimulator leads from Boston Scientific have been recalled after more than 1,000 serious injuries were linked to fractures that may disrupt stimulation and require additional surgery.MORE ABOUT: SPINAL CORD STIMULATOR LAWSUITJudge Allows Back Stimulator Lawsuits Against Boston Scientific to Be Directly Filed in MDL (08/31/2026)Hearing on Abbott, Nevro SCS Lawsuit MDL Centralization Set for September 2026 (08/26/2026)Judge Appoints Spinal Cord Stimulator Lawyers to Leadership Roles in Boston Scientific MDL (08/24/2026) Olympus Scope Wrongful Death Lawsuit Filed Over ERCP Infection (Posted: yesterday)A Kentucky man says his wife died of sepsis and infection complications linked to an Olympus endoscope used during an ERCP procedure.MORE ABOUT: SCOPE INFECTION LAWSUITOlympus Colonoscopy Lawsuit Over C. Diff Infection Set for Status Hearing in September 2026 (08/27/2026)Endoscope Lawsuit Filed Against Fujifilm After Equipment Failure Leads to Injuries (08/24/2026)Colonoscopy Infection Lawsuit Filed Over Contaminated Olympus Scope (07/14/2026) Cartiva Injury Lawyers Appointed to Leadership Roles in Federal MDL (Posted: 2 days ago)A federal judge has appointed more than a dozen plaintiffs’ attorneys to serve in leadership positions in the developing Cartiva lawsuit litigation.MORE ABOUT: CARTIVA IMPLANT LAWSUITCartiva Implant Lawyers To Meet With MDL Judge for Initial Conference in Aug. 2026 (06/30/2026)Failed Cartiva Implant Required Multiple Toe Surgeries, Lawsuit Alleges (06/11/2026)Cartiva Surgery Lawsuit Claims SCI Implant Failure Required Big Toe Fusion (05/26/2026)
Hip Replacement Lawsuit Claims System Failure Caused Woman To Suffer โDusky Metal Diseaseโ June 5, 2026
Boston Scientific Spinal Cord Stimulator Lead Recall Issued After More Than 1,000 Serious Injuries (Posted: today)Certain Infinion CX spinal cord stimulator leads from Boston Scientific have been recalled after more than 1,000 serious injuries were linked to fractures that may disrupt stimulation and require additional surgery.MORE ABOUT: SPINAL CORD STIMULATOR LAWSUITJudge Allows Back Stimulator Lawsuits Against Boston Scientific to Be Directly Filed in MDL (08/31/2026)Hearing on Abbott, Nevro SCS Lawsuit MDL Centralization Set for September 2026 (08/26/2026)Judge Appoints Spinal Cord Stimulator Lawyers to Leadership Roles in Boston Scientific MDL (08/24/2026)
Olympus Scope Wrongful Death Lawsuit Filed Over ERCP Infection (Posted: yesterday)A Kentucky man says his wife died of sepsis and infection complications linked to an Olympus endoscope used during an ERCP procedure.MORE ABOUT: SCOPE INFECTION LAWSUITOlympus Colonoscopy Lawsuit Over C. Diff Infection Set for Status Hearing in September 2026 (08/27/2026)Endoscope Lawsuit Filed Against Fujifilm After Equipment Failure Leads to Injuries (08/24/2026)Colonoscopy Infection Lawsuit Filed Over Contaminated Olympus Scope (07/14/2026)
Cartiva Injury Lawyers Appointed to Leadership Roles in Federal MDL (Posted: 2 days ago)A federal judge has appointed more than a dozen plaintiffs’ attorneys to serve in leadership positions in the developing Cartiva lawsuit litigation.MORE ABOUT: CARTIVA IMPLANT LAWSUITCartiva Implant Lawyers To Meet With MDL Judge for Initial Conference in Aug. 2026 (06/30/2026)Failed Cartiva Implant Required Multiple Toe Surgeries, Lawsuit Alleges (06/11/2026)Cartiva Surgery Lawsuit Claims SCI Implant Failure Required Big Toe Fusion (05/26/2026)