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US Drug Watchdog Now Urges All Transvaginal Mesh Failure Victims That Have Erosion Or A Failed Repair Surgery To Call Them For The Names Of Top Attorneys Who Are Women
Date:4/17/2013

(PRWEB) April 17, 2013

The US Drug Watchdog says,"Our goal is to ensure all transvaginal mesh failure victims who now have erosion, or have undergone a unsuccessful revision surgery to repair a failed transvaginal mesh get to the best possible attorneys, and because the damages are so severe, and gender specific we will do everything possible to make sure the attorneys are all women." According to court records, "A transvaginal mesh failure occurs when the mesh fails to bind to a woman's pelvic tissues. As a consequence of this, the body rejects the mesh that has been sewn into it. As a result, the transvaginal mesh may start to poke its way through the vaginal wall and protrude out of the vaginal tissue. This complication is more commonly referred to as "erosion." Erosion may result in extreme pain, infection, bleeding, vaginal discharge, with no possibility for sexual intercourse." The US Drug Watchdog has begun a very aggressive initiative designed to assist all women across the United States, who are victims of a transvaginal mesh failure involving erosion, or a unsuccessful repair surgery, also known as a revision surgery, and the group is promising the attorneys they recommend will all be women. The group is urging any woman, who has had a transvaginal mesh surgical procedure done, and now has developed severe complications to call them anytime at 866-714-6466.

According to the US Drug Watchdog, "Symptoms of a transvaginal mesh failure may include, pain during sexual intercourse caused by erosion, mesh erosion through the vagina (the mesh is actually protruding out of the vaginal wall), vaginal bleeding, vaginal Infection, urinary problems, organ perforation." http://USDRugWatchdog.Com
The US Drug Watchdog says, "One of the biggest problems we have with respect to our failed medical device or recalled drug initiative work is the average US consumer never hears about a drug recall or failures involving medical devices like a transvaginal mesh failure. If you have a friend, or loved one who is a recipient of a transvaginal mesh that has already failed, please have them call us at 866-714-6466. We want to emphasize this is a nationwide problem impacting women in every US state including California, New York, Ohio, Washington, Massachusetts, Indiana, Georgia, Florida, and all other states. We also want to make certain these victims get to the best possible attorneys to ensure they get the best possible compensation for their transvaginal mesh ordeal, and we will do our absolute best to make certain all of the attorneys are women." http://USDrugWatchdog.Com

U.S. District Court for the Southern District of West Virginia Multidistrict litigation (MDL) consolidates all similar cases into one courtroom and will include the Defendants:
C.R. Bard, Inc., (MDL No. 2187);
American Medical Systems Inc., MDL No. 2325);
Boston Scientific Corp., (MDL No. 2326); and Johnson & Johnson's Ethicon, Inc. (MDL No. 2327)

Read the full story at http://www.prweb.com/releases/2013/4/prweb10620534.htm.


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