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Transvaginal Mesh Lawsuit News: Federal Plaintiff Allowed to Pursue Claims Related to Use of Prolene in Ethicon Mesh Products, Bernstein Liebhard LLP Reports
Date:7/14/2014

New York, NY (PRWEB) July 14, 2014

The federal judge overseeing thousands of Ethicon transvaginal mesh lawsuits (http://www.transvaginalmeshlawsuithelp.com/) has ruled that plaintiffs in one case will be able to pursue certain claims involving the company’s use of a material called Prolene in some of its pelvic mesh devices, Bernstein Liebhard LLP reports. According to an Order dated July 8, 2014, U.S. District Judge Joseph R. Goodwin of the Southern District of West Virginia ruled that the claims are not preempted because the U.S. Food & Drug Administration (FDA) never categorically approved the material for use in medical devices. Instead, the agency only cleared Prolene in relation to its use as a suture, and “did not examine whether that same material was safe when woven together to create a transvaginal mesh product.” (Edwards, et al. v. Ethicon Inc., et al., No. 2:12-9972)

“Our Firm is representing hundreds of women in the Southern District of West Virginia who allegedly suffered serious vaginal mesh complications due to products manufactured by Ethicon, Inc. and other companies. We have been monitoring this issue closely,” says Bernstein Liebhard LLP, a nationwide law firm representing victims of defective drugs and medical devices. The Firm is currently offering free legal evaluations to women who allegedly suffered mesh erosion, pain, scarring, infection and other serious injuries following the implantation of surgical mesh to treat pelvic organ prolapse or stress urinary incontinence.

Ethicon Vaginal Mesh Lawsuits
Ethicon, Inc., a division of Johnson & Johnson, is named a defendant in nearly 20,000 transvaginal mesh lawsuit now pending in the Southern District of West Virginia. All of
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