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Transvaginal Mesh Lawsuit News: Bernstein Liebhard LLP Notes Order Reopening Discovery in Federal C.R. Bard Vaginal Mesh Litigation
Date:5/13/2013

New York, New York (PRWEB) May 13, 2013

Transvaginal mesh lawsuits involving products manufactured by C.R. Bard, Inc. continue to move forward in a multidistrict litigation underway in U.S. District Court, Southern District of West Virginia, Bernstein Liebhard LLP reports. According to an Order issued on May 2nd, the Court has reopened discovery in the proceeding to allow for the deposition of a C.R. Bard executive regarding the alleged use of a prohibited raw polypropylene resin in its mesh products. In doing so, the Court found that the “sheer volume of the production” had prevented plaintiffs from previously discovering emails from the executive that discussed the resin. (In re: C.R. Bard, Inc., Pelvic Repair Systems Products Liability Litigation “MDL No. 2187”)

“We are pleased the Court agreed to reopen discovery in this litigation. We look forward to the continued deposition of this witness,” says Bernstein Liebhard LLP, a nationwide law firm representing victims of defective drugs and medical devices. Firm partner, Jeffrey S. Grand, is serving on the Plaintiffs’ Steering Committee in the federal C.R. Bard vaginal mesh litigation.

C.R. Bard Vaginal Mesh Lawsuits

Pelvic mesh products manufactured by C.R. Bard and other companies have been the subject of growing litigation since October 2008, when the U.S. Food & Drug Administration (FDA) revealed that it had received more than 1,000 reports of serious vaginal mesh injuries over a three year period. In July 2011, the FDA warned that there had been a five-fold increase in reports of serious complications associated with the use of pelvic mesh in prolapse repair since the 2008 alert. According to the agency, the most frequently-reported injuries include mesh erosion through vaginal tissue, infect
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