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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

  • 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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