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Transvaginal Mesh Lawsuit News: FDA Rejects Petition Seeking Ban and Global Recall of All Transvaginal Mesh Products, Bernstein Liebhard LLP Reports
Date:7/25/2014

New York, New York (PRWEB) July 25, 2014

As thousands of transvaginal mesh lawsuits (http://www.transvaginalmeshlawsuithelp.com/) move forward in U.S. courts, Bernstein Liebhard LLP notes that the Food & Drug Administration (FDA) has rejected a petition by the consumer advocacy group, Public Citizen, to order a global recall of all transvaginal mesh products. In a letter dated May 1, 2014, and released to the public last week, the agency also rejected the group’s petition for a ban on the marketing of all surgical mesh devices used in the transvaginal repair of pelvic organ prolapse. According to the letter, the FDA agreed that the use of such products in prolapse repair is associated with post-operative complications such as mesh exposure and extrusions, vaginal scarring, pelvic pain, and infection. However, the letter maintained that a transvaginal mesh recall or ban is not warranted at this time.*

“Our Firm is representing hundreds of women who allegedly suffered many of the vaginal mesh complications noted in the Public Citizen letter. We have been monitoring this matter closely,” says Bernstein Liebhard LLP, a nationwide law firm representing victims of defective drugs and medical devices. The Firm continues to offer free transvaginal mesh lawsuit reviews to women who suffered mesh erosion, pain, scarring, infection and other serious injuries, allegedly due to products manufactured by American Medical Systems, Inc., Boston Scientific Corp., C.R. Bard, Inc. and Ethicon, Inc.

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