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US Drug Watchdog Now Offers Victims Of A Transvaginal Mesh Product Failure A Unequaled Service By Offering the Names of Top Plaintiffs Attorneys-Who are all also Women

(PRWEB) December 18, 2012

The US Drug Watchdog fears there could be thousands of US women recipients of a transvaginal mesh type product that has failed. These specific types of medical products include what are called bladder slings, transvaginal mesh, or tape. The US Drug Watchdog is now offering the names of the best possible lawyers, who are also women to help all US women, who are victim's of a transvaginal mesh, tape, or bladder sling failure. As a background, according to court records transvaginal mesh products were designed for women, who were suffering from pelvic organ prolapse, and or stress urinary incontinence. The procedure to install a transvaginal was supposed to be minimally-invasive. The US Drug Watchdog says, "The FDA is now saying transvaginal mesh product failures are causing complications in patients such as erosion and infection. Women who experience transvaginal mesh failure may need to have numerous corrective surgeries." The US Drug Watchdog has expanded their national initiative designed to help women recipients of transvaginal mesh, tape, or a bladder sling, who are now severely injured by these types of medical products, because they sense a great need for such a service. For more information women, who are victims of a transvaginal mesh, tape or bladder sling product failure are urged to contact the US Drug Watchdog anytime at 866-714-6466. http://USDrugWatchdog.Com

The US Drug Watchdog says, "Symptoms of a transvaginal mesh, tape, or bladder sling 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 Infections, urinary problems, and or non stop urinary tract infections, organ perforation, injury to nearby organs, or severe Pelvic Pain." 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 transvaginal mesh type medical products. If you have a friend, or loved one who is a recipient of a transvaginal mesh, tape, or bladder sling product that has already failed or is showing symptoms of a failure, please have them call us at 866-714-6466. We want to make certain all women, who are transvaginal tape, mesh, or bladder sling failure victims get to the best possible attorneys, to ensure they get the best possible compensation for their 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)

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