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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.
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
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.
Change Healthcare Lawsuit Lawyers are reviewing Change Healthcare class action lawsuits for individuals who had their personal information stolen due to the data breach.
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.
AngioDynamics Port Catheter 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.
Processed Food Lawsuit Lawsuits are being pursued against the food industry over their manufacturing and advertising of ultra-processed foods, which have caused a generation of children to face an increased risk of developing childhood diabetes and other chronic illnesses.
Motion Filed to Consolidate Stryker Rejuvenate Modular Hip Lawsuits February 20, 2013 Austin Kirk Add Your Comments A request has been filed with the U.S. Judicial Panel on Multidistrict Litigation (JPML) to consolidate all federal product liability lawsuits over the Stryker Rejuvenate and ABG II modular-neck stem hip replacement systems, asking that the litigation be centralized before one judge for coordinated handling during pretrial proceedings. There are currently at least 30 Stryker Rejuvenate or ABG II modular hip lawsuits pending throughout the federal court system, with cases spread among 12 different U.S. District Couts. In a motion (PDF) filed on February 12, one of the plaintiffs involved in the litigation, Robert Davis, indicates that the lawsuits should be consolidated as part of a Stryker Rejuvenate MDL, or multidistrict litigation. Such centralization is designed to reduce duplicative discovery among a large number of similar cases, avoid conflicting rulings from different judges and to serve the convenience of the parties, witnesses and the courts. Learn More About Hip Replacement Lawsuits If you or a loved one experienced complications or needed revision surgery due to a defective hip implant, you may be entitled to financial compensation. Learn More SEE IF YOU QUALIFY FOR COMPENSATION Learn More About Hip Replacement Lawsuits If you or a loved one experienced complications or needed revision surgery due to a defective hip implant, you may be entitled to financial compensation. Learn More SEE IF YOU QUALIFY FOR COMPENSATION Davis has asked that the Stryker Rejuvenate litigation be transferred to the U.S. District Court for the District of Minnesota, where at least 10 of the current federal lawsuits are pending. Stryker Rejuvenate Recall Could Result in Sizable Litigation All of the complaints involve allegations that plaintiffs experienced problems with the Stryker Rejuvenate or ABG II modular-neck stem, which was recalled in July 2012 amid reports of corrosion, fretting and early failure. Unlike traditional hip implants, which feature a single femoral component, the Stryker Rejuvenate and ABG II are modular, featuring two pieces that fit inside each other to allow the surgeon to customize the length 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. A Stryker Rejuvenate recall was issued in July 2012, only four years after the hip replacement system was introduced, citing data that indicated a trend of failures. More than 53,000 Stryker Rejuvenate or ABG II modular-neck stems were sold before the recall, most of which had already been implanted in patients. In January 2013, Stryker issued a follow up statement to physicians and consumers, providing updated information and recommendations for individuals who have one of the recalled Rejuvenate or ABG II stems, indicating that regular testing is necessary, even for those patients not yet experiencing device failure. Although there are only 30 cases currently filed in the federal court system, it is widely believed the hundreds, if not thousands, of product liability lawsuits will be filed on behalf of individuals who experience problems with a Stryker Rejuvenate hip. “Moving Party anticipates that the number of currently filed cases is just the beginning of a sizeable litigation,” wrote attorneys for Davis in the motion filed with the U.S. Judicial Panel on Multidistrict Litigation. “Since the recall, the number of adverse events reported to the FDA has increased tremendously. [In addition], Defendant’s evolving recommendations to both surgeons and patients implanted with these devices evidence a growing concerns about the device’s failure rate.” Similar consolidation has already been established in the New Jersey state court system, where all Stryker Rejuvenate lawsuits have been consolidated as part of a Multi-County Litigation (MCL) in Bergen County. A large number of complaints are expected to be filed in New Jersey, as that is the home state for the device manufacturer, Howmedica. The U.S. JPML has not yet established the deadline for Howmedica to respond to the motion for the federal court to establish a Stryker Rejuvenate MDL, and it is not likely that oral arguments will be heard on the motion until an upcoming hearing session scheduled in Chicago on May 30, 2013. Tags: Stryker, Stryker Hip Replacement, Stryker Rejuvenate Image Credit: | More 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 0 Comments 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 No Post Comment I authorize the above comments be posted on this page Weekly 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 TermNameThis field is for validation purposes and should be left unchanged. Δ MORE TOP STORIES BioZorb Implant Removal Surgery: What Women Need To Know When the Device Fails To Dissolve (Posted: today) Following a Class I recall, more than 100 BioZorb lawsuits have been filed by breast cancer survivors who suffered painful complications after the surgical tissue marker failed to dissolve as intended. 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