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.
Registration of Stryker Rejuvenate Hip Cases Required Following Settlement November 17, 2014 Austin Kirk Add Your CommentsFollowing a recent global Stryker Rejuvenate settlement, which is intended to resolve thousands of cases over the recalled hip implant, a federal judge has ordered the registration of all potential claims, regardless of whether they have yet been filed.There are currently about 5,000 Stryker Rejuvenate and ABG II hip lawsuits filed in state and federal courts nationwide, each involving problems experienced after receiving the modular implants, often resulting in the need for revision surgery to remove the defective implant.There were more than 20,000 of Rejuvenate and ABG II implants sold before a Stryker recall was issued in July 2012, when it was determined that the modular neck stem components pose an unreasonable risk of fretting, corroding and ultimately failing as the metal parts rub against each other.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 MoreIn a Pretrial Order (PDF) issued last week, U.S. District Judge Donovan Frank indicating that all lawyers involved in the litigation must register their Stryker Rejuvenate hip cases, including both filed and un-filed lawsuits, as well as claims for individuals who have not yet required revision surgery.Judge Frank is presiding over all federal cases involving the Stryker Rejuvenate or ABG II implants, which have been centralized as part of a multidistrict litigation (MDL) in the U.S. District Court for the District of Missouri. However, the order was issued in cooperation with the litigation in New Jersey state court as well as other state courts nationwide.Following a status conference before Judge Frank, the order was issued to “effectuate the provisions of the private Settlement Agreement,” requiring that all filed and unfiled claims relating to the ABG II Modular Neck Hip Stem or Rejuvenate Modular Neck Hip Stem be identified.The settlement is expected to result in a base payment of $300,000 for each Stryker Rejuvenate or ABG II plaintiff who underwent revision surgery on or before November 2, and otherwise qualifies for the settlement. However, there will be several factors that may reduce the base award, including the plaintiffโs age, prior hip revision surgeries and other related health conditions. In addition, individuals who suffered catastrophic injuries will be able to pursue additional compensation under the settlement if they meet several eligibility requirements for โenhancements.โ“While registration is mandatory pursuant to this Court order, uploading the Registration Declaration and Registration List on the claim processorโs website in no way signifies a claimants commitment or intent to enroll in the settlement program,” wrote Judge Frank in the order.The Stryker Rejuvenate case registration opened on November 14, and lawyers are required to submit complete lists by December 14. For each case, lawyers must provide certain information about the client, as well as designate a Primary Law Firm and appropriate contact information. Following registration, claimants who wish to accept the terms of the settlement must enroll in the program between January 15, 2015 and March 2, 2015.Unlike traditional hip implants, which feature a single femoral component, the Stryker Rejuvenate and ABG II implants featured 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. As the chromium-cobalt components rubbed against each other during normal daily activities, the implant design has been found to release microscopic metal debris, which can lead to failure of the implant.Although the settlement only applies to cases that have required revision surgery by November 2, given the high failure rate with Stryker Rejuvenate hips, it is ultimately expected that new cases will continue to be filed over the next few years, and it is possible that additional settlements will be reached.Judge Frank has indicated that after submitting the Complete Registration Declarations and lists, lawyers are obligated to serve an updated Report if there are any changes in the status of the cases, including if cases are subsequently filed or if the hip patients end up requiring revision surgery in the future. Tags: Hip Replacement System, 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 CommentsCompanyThis 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 Judge Clears Bard PowerPort Lawsuit for Trial, Rejecting Motion for Summary Judgment (Posted: yesterday)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: 2 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) Lawyers Preparing 35 Suboxone Tooth Decay Lawsuits in Core Discovery Pool (Posted: 3 days ago)Nearly three dozen Suboxone tooth decay lawsuits are being prepared for early test trials, involving the deposition of plaintiffs who say they suffered tooth loss as a result of using the opioid addiction treatment.MORE ABOUT: SUBOXONE TOOTH DECAY LAWSUITSuboxone Manufacturer Faces Nearly 18,000 Dental Erosion Lawsuits (07/09/2026)Suboxone Dry Mouth Lawsuit Claims Dental Problems Could Have Been Avoided With Sublocade Shot (06/18/2026)Suboxone Dental Erosion Lawsuit Alleges Indivior Should Have Known About Tooth Decay Risks (06/11/2026)
Hip Replacement Lawsuit Claims System Failure Caused Woman To Suffer โDusky Metal Diseaseโ June 5, 2026
Judge Clears Bard PowerPort Lawsuit for Trial, Rejecting Motion for Summary Judgment (Posted: yesterday)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: 2 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)
Lawyers Preparing 35 Suboxone Tooth Decay Lawsuits in Core Discovery Pool (Posted: 3 days ago)Nearly three dozen Suboxone tooth decay lawsuits are being prepared for early test trials, involving the deposition of plaintiffs who say they suffered tooth loss as a result of using the opioid addiction treatment.MORE ABOUT: SUBOXONE TOOTH DECAY LAWSUITSuboxone Manufacturer Faces Nearly 18,000 Dental Erosion Lawsuits (07/09/2026)Suboxone Dry Mouth Lawsuit Claims Dental Problems Could Have Been Avoided With Sublocade Shot (06/18/2026)Suboxone Dental Erosion Lawsuit Alleges Indivior Should Have Known About Tooth Decay Risks (06/11/2026)