(PRWEB) December 20, 2012
The US Drug Watchdog intends to dramatically expand the scope of their transvaginal mesh product failure initiative in 2013, because the group is convinced most women victims have yet to be discovered. Based on the daily calls they receive, the US Drug Watchdog fears thousands of US women are living in pain almost impossible to comprehend. From what the group hears from victims, the worst part is the physician, or surgeon who did the initial procedure in most cases will not return the frantic phone calls of the recipient of the transvaginal mesh product, or the recipient is being told a severe complication such as mesh protruding through the vaginal wall is, quote normal. The US Drug Watchdog says, "A transvaginal mesh product protruding through the vaginal wall is not normal, nor is it a good thing. 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." The US Drug Watchdog is offering to help all US women, who are victim's of a transvaginal mesh, tape or bladder sling failure get to the best possible attorneys, and the group is promising the attorneys will all be women. For more information victims of a transvaginal mesh, tape or sling 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. Does any of this sound normal?" 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 a transvaginal mesh. 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 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)
Read the full story at http://www.prweb.com/releases/2012/12/prweb10233502.htm.
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