(PRWEB) April 29, 2013
The US Drug Watchdog is now offering to help any victim of a transvaginal failure involving erosion, or an unsuccessful revision surgery get to the best possible attorneys, and the group is promising the attorneys will all be women, because the damages are so severe, and gender specific. 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 mesh was supposed to be minimally-invasive. The 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, IV therapy, blood transfusions and drainage of hematomas or abscesses. The US Drug Watchdog is trying to do everything possible to identify women who have been severely injured by a transvaginal mesh failure, in order to make certain these victims get to the best possible lawyers. 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.
The US Drug Watchdog is indicating symptoms of a transvaginal mesh 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 such as transvaginal mesh. We also need to emphasize there are victims in every state from California to New York, from Washington, to Massachusetts, Florida, Ohio, Texas, Nebraska, Alabama, Idaho, Pennsylvania, etc. If you have a friend, or loved one who is a recipient of a transvaginal mesh implant 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 severely injured by a transvaginal mesh failure 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 lawyers 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)