(PRWEB) May 01, 2013
The US Drug Watchdog is now urging victims of a transvaginal mesh failure involving severe medical complications to call them for the names, and contact information for national caliber women lawyers, because these victims deserve the best possible compensation, and because the group believes women lawyers will be ferocious in taking on the medical device companies involved in this mess. The US FDA is now saying transvaginal mesh, tape, or sling failures are causing complications in patients such as erosion and infection. Women who experience transvaginal mesh failure may need to have numerous corrective surgeries. 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 now saying, "Symptoms of a transvaginal mesh, tape, or sling implant failure may include: severe 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, and or non stop UTI's, 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. Transvaginal mesh failures are a nationwide problem impacting women coast to coast, from Massachusetts, to Washington, from New York to California, Ohio, Florida, Texas, Nebraska, Kansas, and every other state. 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)
Read the full story at http://www.prweb.com/releases/2013/5/prweb10674313.htm.
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