The group is offering to help all US women, who are now victim's of a transvaginal mesh failure get to the best possible attorneys, and the group is promising the attorneys will all be women
(PRWEB) September 24, 2012
The US Drug Watchdog believes transvaginal mesh, or sling failures may be one of the largest, and worst medical device failures for US women-ever. The group is offering to help all US women, who are now victim's of a transvaginal mesh failure get to the best possible attorneys, and the group is promising the attorneys will all be women, because of the very sensitive nature of a transvaginal mesh failure. According to court records transvaginal mesh products were designed for women, who were suffering from pelvic organ prolapse, and or stress urinary incontinence. According to court records the procedure to install a transvaginal was supposed to be minimally-invasive. The US Drug Watchdog now says, "The FDA is now saying transvaginal mesh failures is causing complications in patients such as erosion and infection. Women who experience transvaginal mesh failure may need to have numerous corrective surgeries, IV therapy, blood transfusions and drainage of hematomas or abscesses." The US Drug Watchdog is now expanding their national initiative designed to help women recipients of transvaginal mesh, that is also called a sling, who are now severely injured by these types of medical products. For more information women, who are victims of a transvaginal mesh failure are urged to contact the US Drug Watchdog anytime at 866-714-6466, for the names and contacts of the best possible attorneys-who will all be women. http://USDrugWatchdog.Com
The US Drug Watchdog says symptoms of a transvaginal mesh/Sling implant 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, hardening of the vaginal mesh, injury to nearby organs, and or severe pelvic pain."
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 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 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)