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US Drug Watchdog Now Urges Women Victims Of A Transvaginal Mesh Product Failure Who Had A Unsuccessful Revision Surgery To Call Them For The Names Of Top Women Lawyers
Date:2/1/2013

(PRWEB) February 01, 2013

The US Drug Watchdog is now urging women who are victims of a transvaginal mesh, tape, or bladder sling failure to call them for the names of national caliber lawyers, who are also women; especially if the victim has already undergone a unsuccessful surgery to correct the problem. According to court records, "A transvaginal mesh, tape, 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, bleeding, or vaginal discharge." The US Drug Watchdog says, "We believe the damages we are frequently talking about with a transvaginal mesh, tape, or bladder sling failure victim are almost impossible to comprehend. We are talking about severe injuries like erosion, and we want to make certain all victims at least initially talk to a skilled national caliber woman attorney because the damages are so severe, and gender specific." For more information victims of a transvaginal mesh product 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 bladder 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
  • Hardening of the vaginal mesh
  • Nearby organ injury
  • 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 product. Because a transvaginal mesh, tape, or bladder sling failure is such a sensitive topic we fear the national news media will never adequately cover this vital news story. If you have a friend, or loved one who is a recipient of a transvaginal mesh, tape, or bladder sling 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 product 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/2013/2/prweb10356361.htm.


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