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US Drug Watchdog Now Grows Their Initiative For All US Women Who Are Victims Of A Transvaginal Mesh Product Failure That IncludesThe Names Of Top Women Attorneys To Help
Date:1/9/2013

problems (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 product. Because a transvaginal mesh, tape or 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 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/2013/1/prweb10286186.htm.


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