(PRWEB) January 09, 2013
The US Drug Watchdog has expanded their very aggressive national initiative focused on identifying all US women, who are victims of a transvaginal mesh, tape, or bladder sling failure, and the unique aspect of this initiative is the group will only offer the names of national caliber attorneys-who are also women. Just to get a sense of the potential size of transvaginal mesh, tape, or bladder sling failures, according to the New York Times, "Transvaginal mesh products were designed for women, who were suffering from pelvic organ prolapse, or stress urinary incontinence, and the procedure to install a transvaginal was supposed to be minimally-invasive. In 2010, 185,000 US women had transvaginal mesh type product surgical procedure." The US FDA is now saying, "Transvaginal mesh failures are causing complications in patients such as erosion and infection. Women who experience transvaginal mesh failure may need to have numerous corrective surgeries, blood transfusions and drainage." The US Drug Watchdog has expanded their national initiative designed to help women recipients of transvaginal mesh, tape, or bladder sling, who are now severely injured by these types of medical product-because they fear there is a great need for their very unique service. For more information women, who are victims of a transvaginal mesh product failure are urged to contact the US Drug Watchdog anytime at 866-714-6466. http://USDrugWatchdog.Com
The US Drug Watchdog is indicating symptoms of a transvaginal mesh, tape, or bladder sling implant failure may include:
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 product. Because a transvaginal mesh, tape or sling failure is such a sensitive topic we fear the national news media will never adequately cover this vital news story. If you have a friend, or loved one who is a recipient of a transvaginal mesh, tape or 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 mesh product 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)
Read the full story at http://www.prweb.com/releases/2013/1/prweb10286186.htm.
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