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Transvaginal Mesh Lawsuit News: Bernstein Liebhard LLP Comments on Opening Statements in First Federal C.R. Bard Surgical Mesh Lawsuit Bellwether Trial
Date:7/10/2013

New York, NY (PRWEB) July 10, 2013

Bernstein Liebhard LLP notes that the first federal bellwether trial of a surgical mesh lawsuit involving C.R. Bard transvaginal mesh products began this week in the U.S. District Court, Southern District of West Virginia. According to a report from Bloomberg.com, during yesterday’s opening statements, an attorney for the Plaintiff told a jury of five women and three men that Bard executives knew the company’s Avaulta products had been made from a resin not fit for use in humans, but concealed the flaw from patients and doctors. The Plaintiff, a public health nurse from Georgia, alleges she suffered transvaginal mesh complications after receiving Bard’s Avaulta Plus implant in 2009 to treat pelvic organ prolapse. According to her complaint, the device caused pelvic and rectal pain, bleeding and bladder spasms that have forced her to undergo several surgeries to remove the implant.* (Cisson v. C.R. Bard Inc., 2:11-cv-00195)

“The allegations in this transvaginal mesh lawsuit echo what we have heard from many of our own clients. Our Firm will be monitoring this bellwether trial very closely, as it may provide clues as to how juries will rule in similar cases,” says Bernstein Liebhard LLP, a nationwide law firm representing victims of defective drugs and medical devices. Firm partner, Jeffery S. Grand, serves on the Plaintiffs Steering Committee in the C.R. Bard litigation underway in the Southern District of West Virginia. Bernstein Liebhard LLP continues to offer free legal consultations to women who allegedly suffered serious transvaginal mesh complications following implantation of devices manufactured by C.R. Bard, Inc., as well as American Medical Systems, Inc., Ethicon, Inc. and Boston Scientific Corp.

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