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Federal Ethicon Trial Scheduled to Begin at the End of August in U.S. District Court, Southern District of West Virginia, Bernstein Liebhard LLP Reports
Date:8/14/2014

es claims that Ethicon failed to adequately warn women about these risks in their marketing of the devices. The implants were defectively designed and inadequately tested prior to entering the U.S. market, plaintiffs similarly allege.

In addition to his work in the federal Ethicon mesh litigation, Mr. Grand is also serving on the Plaintiffs’ Steering Committee in several other proceedings in the U.S. District Court, Southern District of West Virginia. These litigations include: American Medical Systems, Inc. (MDL No. 2325); Boston Scientific Corp., (MDL No. 2326); and C.R. Bard, Inc., (MDL No. 2187).

Mr. Grand has also been appointed Co-Liaison Counsel in two vaginal mesh proceedings involving Ethicon and C.R. Bard in New Jersey’s Atlantic County Superior Court. Last year, he served as a member of the Plaintiffs’ trial team for the first trial in the Ethicon proceeding, which ended in March 2013 with an $11 million damage award to the plaintiff. This case involved a woman who suffered transvaginal mesh complications that occurred after receiving an Ethicon Gynecare Prolift implant. (In re: Pelvic Mesh/Gynecare Litigation, No. 6341-10; In re: Pelvic Mesh Litigation/Bard, No. L-6339-10)

Women who were allegedly injured by transvaginal mesh marketed by Ethicon or another company may be eligible to file a lawsuit that seeks compensation for lost wages, out-of-pocket medical expenses, pain and suffering and other damages. Visit Bernstein Liebhard LLP’s website to learn more about the ongoing transvaginal mesh litigations, or visit the Firm’s Facebook page: https://www.facebook.com/meshlawsuit. To obtain a free, confidential and no-obl
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