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.
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
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.
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.
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.
AngioDynamics Port Catheter 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.
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.
Dupixent Lawsuit Dupixent lawsuits are being investigated for patients who developed rare blood cancers such as cutaneous T-cell lymphoma (CTCL) after receiving injections, alleging that Sanofi and Regeneron failed to warn about the potential risks of immune suppression and delayed cancer diagnosis.
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.
Malpractice Lawsuit Over Bard Avaulta Mesh Filed August 11, 2010 Staff Writers Add Your Comments Another medical malpractice lawsuit has been filed against a West Virginia gynecologist over the use of a Bard Avaulta vaginal mesh, which has allegedly caused the plaintiff to suffer severe permanent injury and disfiguration. The Bard Avaulta malpractice lawsuit was filed against Dr. Mitchell E. Nutt, of Huntington, West Virginia, by Dinana Boerke on June 24 in Cabell Circuit Court. Boerke claims that Nutt negligently implanted part of the Bard Avaulta system into her body to treat pelvic organ prolapse. According to a report in the West Virginia Record, the complaint also includes product liability claims against C.R. Bard and Covidien. Boerke’s claim is one of more than a dozen similar lawsuits filed against Nutt over the use of the Avaulta Anterior and Posterior BioSynthetic Support System. A growing number of lawsuits over Bard Avaulta vaginal mesh have also been filed in courts throughout the United States involving similar allegations that C.R. Bard, the manufacturer, was negligent in the product’s design and in failing to warn patients of possible complications with Bard Avaulta pelvic organ prolapse mesh. Learn More About Vaginal Mesh / Bladder Sling Lawsuits Complications from transvaginal mesh may cause severe injuries. Learn More SEE IF YOU QUALIFY FOR COMPENSATION Learn More About Vaginal Mesh / Bladder Sling Lawsuits Complications from transvaginal mesh may cause severe injuries. Learn More SEE IF YOU QUALIFY FOR COMPENSATION The lawsuit claims Boerke suffered mental and physical pain and suffering, permanent injury, substantial physical deformity and loss of a bodily organ system. She alleges that the implanted mesh was harmful and unwanted. In 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. Last month a petition was filed with the U.S. Judicial Panel on Multidistrict Litigation to consolidate the federal Bard Avaulta litigation in one court for pretrial proceedings. At least 36 federal court cases are currently pending against C.R. Bard over problems with Avaulta vaginal mesh. If an MDL, or multidistrict litigation, is formed, all cases filed in federal district courts throughout the United States will be transferred to one judge. In addition, as Bard Avaulta lawyers continue to review and file additional federal cases in the future, those claims will also be transferred into the MDL. Tags: Bard, Bard Avaulta, Bard Avaulta Mesh, Covidien, Medical Malpractice, Surgical Mesh, Vaginal Mesh, West Virginia More Vaginal Mesh Lawsuit Stories Boston Scientific Mesh Lawsuit Filed Over Complications From Obtryx II Mid-Urethral Sling System December 8, 2025 Study Finds Some Transvaginal Mesh Degrades Within 2 Months After It Is Implanted October 29, 2024 Supreme Court Rejects J&J Bid to Overturn $302M Vaginal Mesh Lawsuit Award February 23, 2023 2 Comments Brenda May 2, 2011 I also had surgery in 1995, I haven’t been able to have sex comfortably with my poor husband since the surgery. We both have suffered tremendously. Now I have an infection once again…and it isn’t going away I am going to have to have surgery again I am sure…the pain and infection is unbearable AMBER August 12, 2010 IN 1995, I HAD A SEVEN HOUR LAPARODOMY SURGERY. SEVERAL SURGONS TOOK TURNS REMOVING AND REPAIRING BOWEL, INTESTIN, APPENDIX, AND A FULL HYSTERECTOMY. THE SURGICAL MESH IS WHATS HOLDING MY ORGANS IN PLACE. I HAVE UNBEARABLE PAIN THAT FEELS LIKE SOMETHING IS TWISTED, AND STUCK. THE PAIN IS SO BAD IM UNABLE TO MOVE. I CANT DO ANYTHING. SOMETIMES THIS LASTS FOR HOURS. WHERVER I AM, IM STUCK THERE. TURNING OVER IN THE BED AT NIGHT CAN ALSO TRIGGER THE PAIN. IT FEELS LIKE MY ORGANS ARE TWISTED, PINCHED AND STUCK. I ALSO AM FILLED WITH ADHESIONS, WHICH THE MESH WAS SUPPOSE TO PREVENT. THE LAST 2004 SURGERY WAS SO BAD, THE SURGEON JUST CLOSED ME UP. SAID SHE KEPT LAYERING AWAY AT THE BOWEL, BUT COULDN’T LOCATE IT. IN FEAR OF KNICKING THE BOWEL, SHE GAVE UP. THIS WAS IN 2004. I HAVE SINCE SUFFERED BOWEL, AND INTESTINAL PAIN ON A DAILY BASIS. IT’S ONLY GOTTEN WORSE. I FEEL THAT THE MESH IS THE REASON FOR MY PAIN AND DISCOMFORT. URLThis 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 No Post Comment I authorize the above comments be posted on this page Weekly 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 Term Δ MORE TOP STORIES Lawsuit Claims Spinal Cord Stimulator Battery Problems Resulted in Removal of Boston Scientific Device (Posted: today) A Florida man has filed a lawsuit alleging that battery-related malfunctions in a Boston Scientific spinal cord stimulator caused severe pain and shocking sensations, which required repeated reprogramming attempts that failed, requiring permanent removal. 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