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.
Wright Conserve Hip Litigation Centralized in MDL February 10, 2012 Staff Writers Add Your CommentsA panel of federal judges has ordered that all federal Wright Conserve hip replacement lawsuits be transferred to one judge for coordinated pre-trial proceedings as part of an MDL, or multidistrict litigation.ย ย On February 8, the U.S. Judicial Panel on Multidistrict Litigation centralized the Wright Conserve hip litigation before U.S. District Judge William S. Duffey, Jr. in the U.S. District Court for the Northern District of Georgia.The move will affect four lawsuits that are currently filed in Arizona, California, Georgia and Utah, but there are another 16 cases filed throughout the country that are also likely to be transferred to the MDL and the number of lawsuits is expected to continue to grow as Wright hip replacement lawyers continue to investigate and review potential cases.Do You Know about…Spinal Cord Stimulator lawsuitsSpinal cord stimulator lawsuits are being investigated for individuals who suffered unnecessary shocks, burns or other problems, often resulting in the need for additional surgery to remove the SCS.Learn MoreSEE IF YOU QUALIFY FOR COMPENSATIONDo You Know AboutโฆSpinal Cord Stimulator lawsuitsSpinal cord stimulator lawsuits are being investigated for individuals who suffered unnecessary shocks, burns or other problems, often resulting in the need for additional surgery to remove the SCS.Learn MoreSEE IF YOU QUALIFY FOR COMPENSATIONAll of the complaints allege that Wright Medical Technology manufactured a defective metal-on-metal hip implant, known as the Conserve Plus, and failed to warn patients about the potential risk that the device may fail within a few years of surgery. Plaintiffs say that the Conserve acetabular cup has a tendency to loosen and fail as metal particles are shed into the body from the metal parts rubbing against each other.Wright Medical and one other plaintiff argued against consolidation. The company claimed that there were not enough cases to warrant the creation of an MDL, or multidistrict litigation. Another plaintiff suggested that all of the cases do not involve common questions of fact, since there were various different components used in the different hip replacement implants.The court disagreed and determined that centralization would prevent duplicative discovery and contradictory pretrial rulings by different judges. Only one claim was excluded from the MDL for not being a good fit with the other cases.Since the FDA approved the Wright metal-on-metal hip replacement system under their controversial 510(k) approval system, more than 200 adverse event reports have been submitted by patients or physicians, which likely only represents a fraction of the total number of problems with Wright hip replacements.The Wright Conserve hip system is a metal-on-metal design, which consists of cast cobalt chromium molybdenum that provides the receptacle for the cobalt chromium molybdenum femoral head. The metal femoral head rotates within the metal monoblock Conserve Cup, which does not have a liner, resulting in the release of metal particles that can cause metal toxicity in the blood, soft tissue and bone. This can result in metallosis, tissue necrosis, pseudotumors and other problems, according to the complaints.In addition to the Conserve system, a number of consumers have filed complaints over problems with the Wright Profemur hip replacement, which involves a femoral stem that may be prone to fracture, break, degrade, fret and ultimately fail, according to allegations raised in a number of other lawsuits. Tags: Metal Hip Replacement, Metal-on-Metal Hip, Metal-on-Metal Hip Replacement, Replacement, Wright Conserve Hip Implant, Wright Conserve Plus Hip Implant, Wright Medical Image Credit: |More Lawsuit Stories Judge Clears Bard PowerPort Lawsuit for Trial, Rejecting Motion for Summary Judgment October 2, 2026 Paraquat Settlement Offers Rejected by Hundreds of Parkinsonโs Disease Plaintiffs October 2, 2026 Walmart Expert Grill Brush Recall Impacts 4.4 Million Over Wire Bristle Ingestion Risk October 2, 2026 1 Comments Howard February 14, 2012 Has anyone filed suit against Smith & Nephew for their Birmingham Hip Resurfacing hip ? This device is metal on metal device that was approved for marketing in the USA in 2006, after first being denied approval in 2004. Metal on metal appears to be potentially hazardous to one’s health. Why are all of these MOM hip devices shelved ? I lived a great healthy, active life before my BHR was put into me; now I am in a wheelchair. 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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)
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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)
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