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SOURCE: Wright & Schulte LLC
Plaintiff is Among Hundreds of Women Who Suffered Serious and Life-Altering Injuries, Allegedly Due to Transvaginal Mesh Products Marketed by C.R. Bard and Other Manufacturers.
Columbus, OH (PRWEB) November 19, 2012
Wright & Schulte LLC, a leading nationwide personal injury law firm, has filed a transvaginal mesh lawsuit on behalf of an Iowa woman allegedly injured by Pelvitex Polypropylene Mesh marketed by C.R. Bard, Inc. The lawsuit, which was filed in the C. R. Bard, Inc. Pelvic System Products Liability Litigation (MDL 2187) now underway in U.S. District Court, Southern District of West Virginia, names C. R. Bard and Sofradim Production SAS as Defendants. (Case No. 2:12-cv-06889)
The C.R. Bard transvaginal mesh litigation is one of five pending in the Southern District of West Virginia before Judge Joseph R. Goodwin. Others include In re: Ethicon, Inc., Pelvic Repair System Products Liability Litigation (MDL No. 2327), In re: American Medical Systems, Inc., Pelvic Repair System Products Liability Litigation (MDL No. 2325); In re: Boston Scientific Corp., Pelvic Repair System Products Liability Litigation (MDL No. 2326); and In Re Coloplast Corp. Pelvic Support System Products Liability Litigation. According to Court records, the first trial in the C.R. Bard transvaginal mesh litigation will begin in February 2013.
Additional transvaginal mesh lawsuits have also been filed in state courts throughout the U.S. This past July, a California jury awarded $5.5 million to a woman who claimed to have suffered serious injuries from a C.R. Bard transvaginal mesh device.
The U.S. Food & Drug Administration (FDA) is currently reviewing the safety of transvaginal mesh products used in the surgical repair of pelvic organ prolapse (POP) and stress urinary incontinence (SUI). In a Public Health Notification issued on July 13, 2011, the FDA concluded that serious injuries associated with surgical mesh for transvaginal repair of POP, including neuromuscular problems, vaginal scarring/shrinkage and emotional problems, were “not rare”. The FDA further concluded that transvaginal POP repair with mesh “does not improve symptomatic results or quality of life over traditional non mesh repair.”
Wright & Schulte LLC offers free lawsuit evaluations to victims of transvaginal mesh injuries. If you or someone you love suffered serious, life-altering complication following implantation of transvaginal mesh, please visit yourlegalhelp.com, or call toll-FREE 1-800-399-0795 to learn more about your options for legal recourse.
About Wright & Schulte LLC
Wright & Schulte LLC, a leading personal injury firm, is dedicated to the belief that America’s legal system should work for the people. Every day, the attorneys of Wright & Schulte LLC stand up for the rights of people who have been injured or wronged by defective drugs and their side effects, complications from defective medical devices, and unsafe consumer products, and fight tirelessly to ensure that even the world’s most powerful corporations take responsibility for their actions. If you’re looking for a law firm that will guarantee the aggressive and personal representation you deserve, please do not hesitate to contact Wright & Schulte LLC today. Free case evaluations are available through yourlegalhelp.com, or call 1-800-399-0795.
Wright & Schulte LLC
812 East National Road
Vandalia, Ohio 45377
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