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Virginia Woman Suffers Serious Injuries from Her Transvaginal Mesh Device, Alleges Parker Waichman LLP in Lawsuit
Date:9/13/2013

New York, NY (PRWEB) September 13, 2013

Parker Waichman LLP, a national law firm dedicated to protecting the rights of victims injured by dangerous drugs and defective medical devices, has filed a lawsuit on behalf of a Virginia woman who alleges that a transvaginal mesh implant seriously injured her. The suit was filed on July 10, 2013, in the U.S. District Court for the Southern District of West Virginia (Case No. 2:13-cv-18634) in the Multidistrict Litigation (MDL) entitled In re: C. R. Bard, Inc. Pelvic System Products Liability Litigation, MDL No. 2187. C.R. Bard, Inc., and Sofradim Production SAS have been named as Defendants.

According to the Complaint, the Plaintiff was implanted with the Uretex TO Trans-obturator Urethral Support System on July 25, 2005. The implant was supposed to help treat stress urinary incontinence (SUI) and pelvic organ prolapse (POP), conditions caused by the weakening of the pelvic wall. Transvaginal mesh products are designed to help support the pelvic wall. The lawsuit, however, alleges that the mesh device was defective and had a flawed design that caused serious, and possibly permanent, injuries. The suit further alleges that the Defendants knew about the dangers of their product but chose not to warn consumers.

Thousands of transvaginal mesh lawsuits have been formulated into six MDLs pending in U.S. District Court for the Southern District of West Virginia. The list is comprised of In Re: Ethicon, Inc., Pelvic Repair Systems Products Liability Litigation, MDL No. 2327; In Re: American Medical Systems, Inc., Pelvic Repair Systems Products Liability Litigation, MDL No. 2325; In Re: C.R. Bard, Inc., Pelvic Repair Systems Products Liability Litigation, MDL No. 2187; In Re: Boston Scientific Corp., Pelvic
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