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Transvaginal Mesh Lawsuit News: Bernstein Liebhard LLP Comments on New Study Finding that Vaginal Mesh Does Not Improve Pelvic Organ Prolapse Cure Rate
Date:9/13/2013

(this.href)" rel="nofollow">U.S. Food & Drug Administration (FDA) revealed that it had received more than 1,000 reports of injuries associated with the devices over a three year period. In July 2011, the FDA issued another warning after the reports of serious complications associated with the use of transvaginal mesh in pelvic organ prolapse repair increased by five-fold. The agency also modified the position it had taken in 2008 regarding frequency of vaginal mesh complications in prolapse repair, stating in the alert that these injuries were not rare.

Court documents indicate that more than 20,000 vaginal mesh lawsuits are pending in federal multidistrict litigations now underway in U.S. District Court, Southern District of West Virginia, all of which allege serious injuries due to the use of transvaginal mesh. Bernstein Liebhard LLP partner, Jeffrey S. Grand, is serving on the Plaintiffs’ Steering Committee in four of those litigations, including: In re: American Medical Systems, Inc., Pelvic Repair Systems Products Liability Litigation - MDL No. 2325; In re: Boston Scientific Corp., Pelvic Repair Systems Products Liability Litigation - MDL No. 2326; In re C.R. Bard Inc. Pelvic Repair System Products Liability Litigation, MDL No. 2187; and In re: Ethicon, Inc. Pelvic Repair Systems Products Liability Litigation - MDL No. 2327.

On August 15th, the federal litigation’s first trial of a transvaginal mesh lawsuit concluded when a woman injured by a by C.R. Bard’s Avaulta Plus device was awarded $2 million. (Cisson v. C.R. Bard Inc., 11-cv-00195) The litigation’s second C.R. Bard trial was to get underway the following week, but an undisclosed settlement was reached in the case just prior to the start of opening arguments. (Queen v. C.R. Bard Inc., 11-cv-00012)

Thousands of vaginal mesh lawsuits filed on behalf of women who were allegedly injured by products marketed by C.R. Bard and Ethicon are also pending in two consolidated litigat
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1. US Drug Watchdog Launches Now Calls Transvaginal Mesh A Disaster For 100,000's of US Women Recipients And Offers The Names and Contacts Of The Best Women Attorneys
2. Johnson & Johnson Violated FDA Order to Halt Sales of Transvaginal Mesh
3. US Drug Watchdog Now Fears the Numbers of Transvaginal Mesh Product Failure Victims Will Grow and They Offer Victims the Names of the Best Lawyers-Who Will All Be Women
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8. US Drug Watchdog Now Urges All Victims of a Transvaginal Sling, Tape, or Mesh Failure to Call Them for the Names of National Caliber Women Attorneys-Get Help Now
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