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.
Initial Conference in Stryker Rejuvenate Hip MDL To Be Held in August July 18, 2013 Austin Kirk Add Your CommentsThe first meeting with the federal judge presiding over all centralized Stryker Rejuvenate hip lawsuits will be held next month, at which time the structure and organization for the consolidated federal multidistrict litigation (MDL) will be discussed.According to a Pretrial Order (PDF) issued on July 5, U.S. District Judge Donovan W. Frank indicates that a Status Conference will be set for a date in August 2013, although the exact date and time have not yet been provided by the Court.In June, the U.S. Judicial Panel on Multidistrict Litigation ordered that all product liability lawsuits filed throughout the federal court system involving problems with Stryker Rejuvenate or Stryker ABG II modular implants will be transferred to Judge Frank for coordinated handling during pretrial proceedings.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 MoreAt the time the Stryker Rejuvenate MDL was established, there were about 41 complaints filed in 16 different U.S. District Courts, but lawyers expect that hundreds, if not thousands, of Stryker hip lawsuits are likely to be filed in the coming months.Centralizing the cases before one judge is designed to reduce duplicative discovery into common issues that will arise in a large number of cases, to avoid conflicting pretrial rulings from different judges and to serve the convenience of the parties, the witnesses and the courts.According to Judge Frank’s order, an interim lead counsel and liaison counsel were appointed for plaintiffs who have brought cases. However, it is expected that a larger group of attorneys will be appointed to leadership roles following the status conference. These lawyers would take certain actions that benefit all plaintiffs who have brought a Stryker Rejuvenate case in the MDL during the discovery phase and pretrial proceedings, including any “bellwether” cases that may be scheduled to help the parties gauge how juries are likely to respond to evidence and testimony that could be repeated throughout a large number of cases.Stryker Rejuvenate RecallA recall was issued for the Stryker Rejuvenate and Stryker ABG II hip replacements in July 2012, after reports suggested that a higher-than-expected number of modular components were failing within a few years after they were implanted. Although artificial hips are expected to last 15 to 20 years, these components were removed from the market only a few years after they were introduced.Unlike traditional hip implants, which feature a single femoral component, the Stryker Rejuvenate and ABG II are modular neck-stems, featuring two pieces that fit inside each other to allow the surgeon to customize the length of the femoral component based on the patient. However, the design has been linked to an increased risk of problems that may result from the release of microscopic metal debris as the chromium-cobalt neck rubs against the titanium femoral stem. This can cause the implants to corrode or fret at the modular junction, increasing the risk of inflammation and loosening of the hip implant.All of the complaints included in the MDL involve allegations that Howmedica and their Stryker subsidiaries designed and sold a defective and unreasonably dangerous system. Complaints also allege that the manufacturer failed to warn patients or the medical community about the potential risk ofย problems with Stryker Rejuvenate hip replacements.Prior to removing the devices from the market, more than 20,000 Stryker Rejuvenate and ABG II hips were sold nationwide. Over the coming months, the size of the Stryker Rejuvenate litigation is expected to increase dramatically as individuals throughout the country continue to experienceย Stryker Rejuvenate hip failures, which often result in the need for revision surgery.Asย product liability lawyers continue to review and file Stryker Rejuvenate casesย in U.S. District Courts throughout the country, they will be transferred to Judge Frank for coordinated handling and pretrial proceedings.In addition to claims pending in the federal MDL, at least 161 lawsuits were consolidated in New Jersey state courts earlier this year, where the cases have been centralized before Judge Brian R. Martinotti in Bergen County. Tags: Metal-on-Metal Hip, Stryker, Stryker ABG II, Stryker RejuvenateMore 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 Depo-Provera Meningioma Side Effects Left Woman With Debilitating Migraines, Lawsuit Claims (Posted: 3 days ago)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: 4 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: 5 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)
Hip Replacement Lawsuit Claims System Failure Caused Woman To Suffer โDusky Metal Diseaseโ June 5, 2026
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Port Catheter Thrombosis Lawsuit Claims Defective AngioDynamics Xcela Device Caused Injury (Posted: 5 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)