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.
Bard Avaulta Surgical Mesh Lawsuits Centralized in MDL October 18, 2010 Staff Writers Add Your CommentsThe U.S. Judicial Panel on Multidistrict Litigation has decided that all federal lawsuits over Bard Avaulta surgical mesh should be consolidated for pretrial litigation in the U.S. District Court for the Southern District of West Virginia.ย The Panel issued an order on October 12, which will result in at least 36 different Bard Avaulta mesh lawsuit claims currently pending in federal courts across the country being transferred to U.S. District Judge Joseph Goodwin in Charleston. In addition, as Bard Avaulta lawyers continue to file new federal cases for complications involving the surgical mesh used during pelvic organ prolapse procedures, they will also be transferred to Judge Goodwin’s court.All of the lawsuits include similar complaints that C.R. Bardโs Avaulta Anterior and Posterior BioSynthetic Support System was negligently designed and that the company failed to warn patients of possible complications that can result in severe pain and disfigurement.Learn More AboutVaginal Mesh / Bladder Sling LawsuitsComplications from transvaginal mesh may cause severe injuries.Learn MoreSEE IF YOU QUALIFY FOR COMPENSATIONLearn More AboutVaginal Mesh / Bladder Sling LawsuitsComplications from transvaginal mesh may cause severe injuries.Learn MoreSEE IF YOU QUALIFY FOR COMPENSATIONIn October 2008, the FDA issued a warning about problems with surgical mesh like the Bard Avaulta. The vaginal mesh products, which are used to treat pelvic organ prolapse (POP) and stress urinary incontinence (SUI), have been associated with over 1,000 reports of severe infection, pain, urinary problems and bowel, bladder or blood-vessel perforations. Many women have also reported recurrences of the prolapse or incontinence, and the need for additional surgeries to remove mesh that had eroded into the vagina.A pelvic organ prolapse occurs when organs such as the bladder, uterus, bowel or rectum drop and push against the wall of the vagina. This happens when the muscles holding the pelvic organ in place become weak or stretched, often due to childbirth or surgery. The surgical mesh is used to support the muscle.Consolidation of the Bard Avaulta surgical mesh lawsuits before one judge as part of an MDL is designed to reduce duplicative discovery, avoid contradictory rulings from different judges and to serve the convenience of the court, witnesses and parties. While the pretrial management of the cases in an MDL is often managed similar to how a Bard Avaulta class action lawsuit would be handled, each claim will still remain an individual lawsuit.ย If an agreement to settle Bard Avaulta lawsuits is not reached during pretrial proceedings, the consolidated cases will be remanded back to the jurisdiction where they were originally filed for trial. Tags: Bard, Bard Avaulta, Bard Avaulta Mesh, Medical Malpractice, Surgical Mesh, Vaginal Mesh, West Virginia Image Credit: |More Vaginal Mesh Lawsuit Stories Boston Scientific Lynx Mesh Lawsuit Alleges Bladder Erosion Required Multiple Surgeries July 28, 2026 Boston Scientific Pelvic Mesh Lawsuit Claims Advantage System Caused Permanent Injury, Deformity June 17, 2026 Boston Scientific Mesh Lawsuit Filed Over Complications From Obtryx II Mid-Urethral Sling System December 8, 2025 2 Comments Sue April 20, 2011 Five years ago I had surgery for a mesh bladder sling. Since that time I have had recurrent (ever 6-8 weeks) since and now have to drug resistant bacteria in my bladder. On two low dose antibiotics for each bacteria that are both colonized. Slowly becoming resistant to all usual antibiotics. Now under the care of an infectious disease doctor who is considering giving me an antibiotic crystal which dissolves in water. I have suffered pain, incontinence, fevers, and infection too numerous to count. I have been told removal of the sling will not now remove the infections which are termed hospital passed infections. Sepsis a real issue and general fatigue, anemia, etc. tom January 30, 2011 i hadd a xenmatrix patch as a result of a cabge in 2009. within 45 days i went into septic shock. i have been in and out of nursing homes and hospitals ever since. the patch was insdtalled at St Joes in Baltimore. It was alledgedly removed at Washington County Hospitasl in Marylant. However when i was transported by air back to St Joes they maintained that the wound was pussey and was not cleaned up as they expected, Nor hav ibeen notified that the xenmatrix was a problem CompanyThis 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. 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