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Transvaginal Mesh Lawyer Applauds PBS Program Questioning FDA’s Approval of Pelvic Mesh Products
Date:3/26/2013

St. Louis, MO (PRWEB) March 26, 2013

Defective medical products lawyer John J. Driscoll today applauded PBS for airing a program about the U.S. Food and Drug Administration’s process for approving medical devices – specifically surgical mesh that is used to treat women with pelvic organ prolapse or stress urinary incontinence.

On PBS’ March 22 episode of “Need to Know,” medical correspondent Dr. Emily Senay examined whether the FDA’s medical device review process is adequately protecting the public. The program specifically focused on pelvic mesh products, which are also known as “transvaginal mesh” or TVM, and women who say they have become disabled after surgical implantation of the devices.

A short summary of the “Need to Know” episode available online features a woman who was diagnosed seven years ago with pelvic organ prolapse (POP), “a condition hundreds of thousands of women face.”

At the advice of her doctor, she had pelvic mesh implanted. However, she began to suffer severe pain immediately after the surgery, according to PBS.

“This PBS program puts a face on the women who are dealing with the debilitating side effects that are alleged to be caused by these mesh products,” Driscoll said.

“At our firm, we know these women through our own work to help them obtain compensation for their medical expenses and for the pain t
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