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US Drug Watchdog Now Urges All Victims Of The Transvaginal Mesh Product Failure To Call Them For The Names Of Top Attorneys-Who Are All Women-Don't Get Ignored Any Longer
Date:1/18/2013

(PRWEB) January 18, 2013

The US Drug Watchdog says, "Ignoring a problem infrequently makes the problem go away. We talk to women everyday about transvaginal mesh, tape, or bladder sling failures, and we are horrified at the lack of response to severe side effects, such as the mesh protruding through the vaginal wall. We are also talking about a potentially huge group of women in the United States. The New York Times has reported in 2010 185,000 US women had a transvaginal procedure done. That was just one year." According to the US FDA, "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. Erosion may result in extreme pain, infection, and bleeding." The US Drug Watchdog's national initiative is designed to assist any women in the US, who is a victim of a transvaginal mesh, tape 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, tape, or sling failure are urged to call the US Drug Watchdog anytime at 866-714-6466. http://USDrugWatchdog.Com

The US Drug Watchdog is indicating symptoms of a transvaginal mesh, tape, or 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
  • UTI's
  • Organ perforation
  • Hardening of the vaginal mesh
  • Injury to nearby organs
  • 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, tape, or bladder sling 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, tape, or bladder sling 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/2013/1/prweb10309113.htm.


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