US Drug Watchdog Now Urges All Victims Of The Transvaginal Mesh Or Tape Failure To Call Them For The Names Of National Caliber Attorneys–Who Are All Women

The US Drug Watchdog has dramatically grown their national initiative focused on helping women recipients of a failed transvaginal mesh, tape, or sling type product, because there could easily be thousands of victims. According to the New York Times, "In 2010, about 185,000 US women underwent procedures in which a mesh type product was implanted vaginally to treat urinary incontinence." The US Drug Watchdog says, "Transvaginal mesh or Bladder Sling failure occurs when the mesh fails to bind to a woman's pelvic tissues. As a consequence of this, the body rejects the mesh that has been sewn into it. As a result, the transvaginal mesh may start to poke its way through the vaginal wall and protrude out of the vaginal tissue. This complication is more commonly referred to as erosion." The US Drug Watchdog's national initiative is designed to assist any women in the US, who is a victim of a transvaginal mesh, or bladder sling failure, and the group will provide all women victims with the specific contacts of national caliber attorneys-who are all women. For more information women, who are now victims of a transvaginal mesh failure are urged to call the US Drug Watchdog anytime at 8660714-6466. http://USDrugWatchdog.Com

The US Drug Watchdog is now expanding their national initiative designed to help women recipients of transvaginal mesh, tape, or sling type products who are now severely injured by these types of medical products

(PRWEB) October 15, 2012

The US Drug Watchdog has designed their Transvaginal Mesh Victims Initiative around the core concept that women victims will get access to the highest caliber national attorneys-who are all women. The US Drug Watchdog does not believe a woman victim of a transvaginal mesh, tape, or sling failure would want to share this type of information with a male attorney. As a background the 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 qoute minimally-invasive. 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, 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, tape, or sling type products 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. 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, severe pelvic pain." 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 failure. If you have a friend, or loved one who is a recipient of a transvaginal mesh product 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)

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