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Transvaginal Mesh Lawsuits Continue, as Bernstein Liebhard LLP Comments on Reported Settlement of American Medical System Vaginal Mesh Lawsuits
Date:6/22/2013

Food & Drug Administration (FDA) issued a public health alert stating there had been a five-fold increase in vaginal mesh complications reported to the agency. In the warning, the FDA also re-classified the frequency of complications stemming from pelvic organ prolapse repair as “not rare,” which was a change from the position it had taken previously.** Since then, a number of women’s groups have called on the FDA to order a transvaginal mesh recall, Bloomberg.com said.

Bernstein Liebhard LLP partner, Jeffrey S. Grand, is serving on the Plaintiffs’ Steering Committee in the federal American Medical Systems litigation, and for several other vaginal mesh proceedings now underway in the Southern District of West Virginia, including: In re: Boston Scientific Corp., Pelvic Repair Systems Products Liability Litigation (“MDL No. 2326); In re: C.R. Bard, Inc., Pelvic Repair Systems Products Liability Litigation (“MDL No. 2187”), and In re: Ethicon, Inc., Pelvic Repair Systems Products Liability Litigation (“MDL No. 2327”). The litigation’s first trial of a transvaginal mesh lawsuit is scheduled to begin on July 8th, and will involve a C.R. Bard claim.

Mr. Grand is also serving as Co-Liaison Counsel in two consolidated litigations underway in New Jersey’s Atlantic County Superior Court involving products manufactured by C.R. Bard and Ethicon. In addition, he was a member of the trial team for the first Ethicon mesh lawsuit trial in that proceeding, which ended in March with an $11 million verdict for the Plaintiff. (In re: Pelvic Mesh/Gynecare Litigation, No. 6341-10; In re: Pelvic Mesh Litigation/Bard, No. L-6339-10)

Women who have allegedly suffered serious transvaginal mesh injuries may be entitled to compensation for their medical bills, pain and suffering, and other injuries. A wealth of informatio
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