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.
Settlements Continue in Stryker Rejuvenate Hip Recall Lawsuits March 4, 2014 Austin Kirk Add Your CommentsAgreements continue to be reached to settle lawsuits brought by individuals who experienced problems with recalled Stryker Rejuvenate hip replacements, as early mediations are on-going in an effort to resolve cases before a lengthy litigation process.According to a case management order (PDF) issued last week in the Superior Court of New Jersey for Bergen County, where nearly 800 Stryker Rejuvenate lawsuits are currently pending, the parties have successfully settled eight out of the first nine cases to go through a court-ordered mediation process.Nearly 1,500 Stryker Rejuvenate hip cases have been filed in state and federal courts throughout the country, all involving similar allegations that problems with the modular design of the hip replacement system caused the implant to fret, loosen and fail within a few years.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 MoreA Stryker hip recall was issued in July 2012, impacting an estimated 20,000 Rejuvenate and ABG II implants that featured similar designs. Although hip implants are expected to last 15 to 20 years, the recall was issued less than two years after the design was introduced, due to a higher-than-expected failure rate.Unlike traditional hip implants, which feature a single femoral component, the Stryker Rejuvenate and ABG II contains a modular neck-stem, which consists of 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.Stryker Rejuvenate Mediation ProgramIn New Jersey state court, all Stryker hip lawsuits have been centralized before Superior Court Judge Brian R. Martinotti in Bergen County, where the cases is being coordinated as part of a Multi-County Litigation, or MCL.In an attempt to see if Stryker Rejuvenate settlements may be reached before lengthy and expensive litigation, Judge Martinotti established a mediation process last year.The first phase involved a group of 10 cases that were selected for early negotiations before a court-appointed mediator. One of those selected cases was delayed, but the parties were able to successfully resolve eight of the remaining nine cases following mediation efforts, Judge Martinotti reported in the order issued February 27.Another group of cases are currently being selected for a second phase of mediation efforts, which will involve several cases where the plaintiffs are 78 years of age or older. The Court has already randomly selected five cases and plaintiffs have identified another five cases that will be part of this phase 2 mediation. Stryker has been ordered to choose it’s selections no later than March 14, 2014.Following the finalization of the second round case picks, the parties will submit all pertinent medical records and a Plaintiff Fact Sheet within 10 days of the selection of the case for mediation.The parties are scheduled to meet with Judge Martinotti for a case management conference on April 1, 2014, at which time it is expected that additional information will become available about the status of the mediation program.In addition to cases pending in New Jersey state court, more than 576 complaints are currently pending in the federal court system, where cases filed throughout the country have been centralized before U.S. District Judge Donovan Frank in the District of Minnesota, as part of an MDL or Multidistrict Litigation.According to a joint status report submitted by the parties in the MDL on February 17, a similar mediation program is being considered in the federal Stryker Rejuvenate MDL, given the success of the New Jersey mediations.If progress towards settlement does not continue, it is likely that small groups of cases will be scheduled for early trial dates. Known as “bellwether” cases, such early trial dates are common in complex medical device litigation, as they could help the parties gauge how juries may respond to certain evidence and testimony that is likely to be repeated throughout the litigation. Tags: Hip Replacement System, New Jersey, Stryker, Stryker ABG II, 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 CommentsEmailThis 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 Bard PowerPort Fracture Lawsuit Set For Second Bellwether Trial in Aug. 2026 (Posted: 2 days ago)The second Bard PowerPort bellwether trial is now scheduled to begin in August after the plaintiff in a claim originally planned for trial next month died, and her family stopped pursuing litigation.MORE ABOUT: BARD POWERPORT LAWSUITJury Returns Defense Verdict in First Bard PowerPort Injury Lawsuit (05/11/2026)Jury Selection Underway in First Bard PowerPort Trial Over Infection Claims (04/16/2026)Judge Blocks Juries From Hearing About IVC Filter Problems in Bard PowerPort Trials (04/08/2026) Dupixent Cancer Lawsuit Claims Eczema Drug Caused Womanโs CTCL Diagnosis (Posted: 3 days ago)A Delaware woman has filed a Dupixent lawsuit, claiming manufacturers promoted the eczema drug as a breakthrough treatment while failing to warn that it may trigger or worsen CTCL, a rare form of non-Hodgkinโs lymphoma.MORE ABOUT: DUPIXENT LAWSUITLink 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)Judges Will Consider MDL for Dupixent Cancer Lawsuits Late Next Month (04/21/2026) Omnipod Recall Impacts Another 7 Million Defective Pods That May Cause DKA, Hospitalization (Posted: 4 days ago)Federal regulators have expanded an Omnipod recall after reports that internal tubing defects may cause insulin leaks and under-delivery, potentially triggering dangerous blood sugar spikes.MORE ABOUT: OMNIPOD RECALL LAWSUITRecalled Omnipod 5 Injuries Skyrocket, Prompting Removal of Insulin Pump Pods (04/30/2026)Insulet OmniPod 5 Recall Lawsuits May Be Filed Over Problems Resulting in Diabetic Ketoacidosis, Hospitalization and Death (03/24/2026)Omnipod 5 Insulin Pump Recall Follows Reports of Serious Injuries: FDA (03/20/2026)
Zimmer Biomet CPT Hip System Linked to Increased Risk of Thigh Bone Fractures, FDA Warns September 18, 2024
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