(PRWEB) October 10, 2012
The US Drug Watchdog has launched a very aggressive initiative designed to help all women recipients of a transvaginal mesh product, or a sling, who are now severely damaged by this type of product. Transvaginal mesh was designed for women, who were suffering from pelvic organ prolapse and stress urinary incontinence. According to the US FDA the procedure to install a transvaginal was supposed to be minimally-invasive. The US Drug Watchdog now says, "The Transvaginal Mesh Disaster is the worst mess we have ever seen for women. The FDA is now saying transvaginal mesh failures is causing complications in patients such as erosion and infection. Patients who experience transvaginal mesh failure have needed corrective surgery, IV therapy, blood transfusions and drainage of hematomas or abscesses." The US Drug Watchdog is offering to help any victim of the transvaginal mesh disaster get to the best possible attorneys, and the group is promising the attorneys will all be women. For more information victims of the Transvaginal Mesh Disaster are urged to contact the US Drug Watchdog anytime at 866-714-6466, or contact the group via their web site at 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 the a transvaginal mesh failure-even if it involves thousands, or tens of thousands of innocent US victims. If you have a friend, or loved one who is a recipient of a transvaginal mesh that has already failed or is showing symptoms of a failure, please have them call us at immediately at 866-714-6466. We want to make certain these Transvaginal Mesh Disaster 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)