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.
Bellwether Categories Established for Stryker Rejuvenate Injury Lawsuits May 15, 2014 Austin Kirk Add Your CommentsAs the litigation involving injuries associated with the recalled Stryker Rejuvenate hip replacements continues, the U.S. District Judge presiding over the lawsuits has indicated that a pool of cases being prepared for early trial dates will be divided into different categories based on the date of the hip implant, specific product received and problems experienced by the plaintiffs.Howmedica Osteonics currently faces more than 2,000 Stryker Rejuvenate injury lawsuits filed by individuals throughout the United States who received a hip replacement involving the modular femoral neck-stems, which were recalled in July 2012 amid reports that the device is prone to fret, corrode and fail within a few years after it is implanted.Unlike traditional hip implants, which feature a single femoral component, the Stryker Rejuvenate and ABG II contained a modular neck-stem, with two pieces that fit inside of 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.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 MoreAlthough hip implants are typically expected to last 15 to 20 years, aย Stryker Rejuvenate recallย was issued less than two years after the design was introduced, and the number of product liability lawsuits filed nationwide continue to increase as problems develop among the estimated 20,000 patients who received the device.Approximately 825 of the cases are currently pending are filed in the federal court system, where the litigation is being overseen by U.S. District Court Judge Donovan Frank in Minnesota federal court. In addition, about another 1,200 complaints are pending in New Jersey state court, which is the home state for the medical device manufacturer.Stryker Rejuvenate Bellwether TrialsAs part of the coordinated pretrial proceedings in the federal court system, a small group of cases are being prepared for early trials, known as “bellwether” cases. These lawsuits are designed to be representative of other complaints in the litigation, and the outcomes are designed to help gauge how juries may respond to certain evidence and testimony that is likely to be similar among a large number of cases.On May 9, Judge Frank issued a pretrial order (PDF) that indicates these early test cases will be divided into five separate categories.There are four categories for those who received Stryker Rejuvenate implants, and one for those who received the ABG II hip system, which is another implant involving the same design that was also recalled in July 2012. Very few of the injury lawsuits filed to date have involved the ABG II implant, with the vast majority involving Stryker Rejuvenate hips.Of the categories involving Stryker Rejuvenate injury claims, the lawsuits will be divided by whether the plaintiff received the implant before or after January 1, 2011, and whether the revision was complicated or uncomplicated. Judge Frank previously determined that all of the bellwether cases will be restricted to plaintiffs who have had to undergo revision surgery to have the implants removed following catastrophic failure or complications that merited its removal.According to an order issued in March 2014, it is expected that between three and five Stryker Rejuvenate bellwether trials will be scheduled in the MDL, with the first cases ready to begin during the summer of 2015. The categories are no indication of what order the cases will be prioritized, Judge Frank clarified this month.Following the bellwether trials, if agreements are not reached to settle or resolve a large number of cases, Judge Frank may begin remanding hundreds of cases back to U.S. District Courts throughout the country for individual trial dates.In Extremis DispositionsThe bellwether order came just two days after Judge Frankย established procedures (PDF) that will allow plaintiffs suffering from severe health problems to preserve their testimony, in the event they are never able to attend their own trial due to health reasons or death.Known as “in extremis” depositions, Judge Frank indicated that plaintiffs must provide a certification or affidavit from their doctor indicating that they are hospitalized, terminally ill or in hospice care because of their medical condition and are not likely to recover before the trial. Plaintiffs’ attorneys must provide defense attorneys with a copy of the plaintiffs medical records, and must also provide a release of records and a number of other necessary fact sheets.New Jersey Mediation Efforts to Settle Stryker Rejuvenate CasesIn 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 ifย Stryker Rejuvenate settlements may be reachedย 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. Tags: Hip Replacement System, Srtryker ABG II, Stryker, Stryker Rejuvenate 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 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 Abbott and Nevro Spinal Cord Stimulator Lawsuits Centralized in New Federal MDLs (Posted: today)Federally filed lawsuits against Abbott Laboratories and Nevro over alleged spinal cord stimulator injuries have been consolidated into two separate multidistrict litigations in California and Illinois.MORE ABOUT: SPINAL CORD STIMULATOR LAWSUITSpinal Cord Stimulator Lawsuit Alleges Boston Scientific Device Failure Required Removal Surgery (09/29/2026)Nevro SCS Implant Lawsuit Alleges Sales Rep Programming Led to Permanent Nerve Damage (09/21/2026)Boston Scientific Spine Stimulator Lawsuit Filed Over Numbness, Incontinence, Erectile Dysfunction (09/16/2026) Judge Clears Bard PowerPort Lawsuit for Trial, Rejecting Motion for Summary Judgment (Posted: 3 days ago)A U.S. District Judge refused to dismiss a Bard PowerPort lawsuit just two weeks before it is supposed to go to trial, saying the manufacturer will have to convince a jury with their arguments and not him.MORE ABOUT: BARD POWERPORT LAWSUITBard PowerPort Infection Lawsuit Set for Third Bellwether Trial to Begin Oct. 13 (09/14/2026)Jury Awards $40M Port Catheter Lawsuit Payout in Bard PowerPort Bellwether Trial (09/09/2026)Nearly 4,000 Bard PowerPort Lawsuits Are Awaiting Outcome of Upcoming Bellwether Trials (08/12/2026) Dupixent Lawyers Seek Leadership Positions in MDL Over Cancer Risks (Posted: 4 days ago)Plaintiffs propose that about a dozen attorneys be appointed to leadership positions in the growing Dupixent cancer litigation.MORE ABOUT: DUPIXENT LAWSUITDupixent Side Effects Lawsuit Alleges Drug Caused Cutaneous T-Cell Lymphoma (09/24/2026)Dupixent Side Effects Caused CTCL, Tumors, Lawsuit Alleges (09/10/2026)Dupixent Lymphoma Lawsuit Alleges Atopic Dermatitis Drug Led to Mycosis Fungoides Diagnosis (08/20/2026)
Hip Replacement Lawsuit Claims System Failure Caused Woman To Suffer โDusky Metal Diseaseโ June 5, 2026
Abbott and Nevro Spinal Cord Stimulator Lawsuits Centralized in New Federal MDLs (Posted: today)Federally filed lawsuits against Abbott Laboratories and Nevro over alleged spinal cord stimulator injuries have been consolidated into two separate multidistrict litigations in California and Illinois.MORE ABOUT: SPINAL CORD STIMULATOR LAWSUITSpinal Cord Stimulator Lawsuit Alleges Boston Scientific Device Failure Required Removal Surgery (09/29/2026)Nevro SCS Implant Lawsuit Alleges Sales Rep Programming Led to Permanent Nerve Damage (09/21/2026)Boston Scientific Spine Stimulator Lawsuit Filed Over Numbness, Incontinence, Erectile Dysfunction (09/16/2026)
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