US Drug Watchdog Now Expands Their Transvaginal Mesh Initiative for All US Victims and They Are Offering the Names of the Best Possible Attorneys-Who Are also Women

The US Drug Watchdog says, "We are calling transvaginal mesh, tape, or sling failures a catastrophe for potentially thousands of US women, with damages that are literally beyond comprehension. According to the New York Times, in 2010, about 185,000 women underwent procedures in which mesh was implanted vaginally to treat urinary incontinence. That is 2010 alone." A transvaginal mesh, tape, or 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 product 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 has expanded their very aggressive initiative designed to assist all victims of a transvaginal mesh, tape, or sling failure-because they are hearing from so many victims. The group is urging any woman, who has had the transvaginal mesh, tape, or sling surgical procedure done, and now has developed severe medical complications to call them anytime at 866-714-6466. As part of their initiative the US Drug Watchdog is offering to send all US women, who are victims of a transvaginal mesh, tape, or sling failure to national caliber attorneys-who are all women. http://USDrugWatchdog.Com

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The US Drug Watchdog has expanded their very aggressive initiative designed to assist all victims of a transvaginal mesh, tape, or sling failure-because they are hearing from so many victims

(PRWEB) November 16, 2012

The US Drug Watchdog has expanded their national initiative designed to help victims of a transvaginal mesh, tape, or sling failure, who are now severely damaged by this type of medical product-because they see a great need for their unique service. Supposedly transvaginal mesh products were designed for women, who were suffering from pelvic organ prolapse, and or stress urinary incontinence. According to the US FDA the procedure to install a transvaginal was supposed to be minimally-invasive. The US Drug Watchdog now says, "The FDA is now saying transvaginal mesh failures is 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 offering to help all US women, who are now victim's of a transvaginal mesh, tape, or sling failure get to the best possible attorneys, and the group is promising-the attorneys will all be women. No other Group is offering a service like this. For more information victims of a transvaginal mesh, tape, or sling failure are urged to contact 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
  • Urinary problems (Non stop urinary tract infections-UTI's)
  • Organ perforation

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 sling failure. If you have a friend, or loved one who is a recipient of a transvaginal mesh, tape, or sling type 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 transvaginal mesh, tape, or 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)


Contact

  • M Thomas Martin
    Americas Watchdog
    866-714-6466
    Email

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