US Drug Watchdog Now Calls The Damages In A Transvaginal Mesh, Tape Or Sling Failure Beyond Comprehension & Offers to Help Victims Get to the Best Possible Women Lawyers

The US Drug Watchdog is describing the daily accounts of damages they get from victims of a transvaginal mesh, tape, or sling failure as almost impossible to comprehend. In some instances they describe the damages as impossible to comprehend. 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 are causing complications in patients such as erosion and infection. Women who experience transvaginal mesh failure, tape, or sling failure may need to have numerous corrective surgeries." 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. Victims of a transvaginal mesh product failure are urged to contact the US Drug Watchdog anytime at 866-714-6466. http://USDrugWatchdog.Com

  • Share on TwitterShare on FacebookShare on Google+Share on LinkedInEmail a friend
The US Drug Watchdog is describing the daily accounts of damages they get from victims of a transvaginal mesh, tape, or sling failure as almost impossible to comprehend

(PRWEB) November 29, 2012

The US Drug Watchdog's Transvaginal Mesh Product Failure Initiative is focused on identifying what they expect to be thousands of US women victims, who are stuck with medical issues that are almost beyond comprehension involving transvaginal mesh, tape, or sling failures. 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." Transvaginal mesh 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." The US Drug Watchdog has begun a very aggressive national initiative designed to make certain every victim of a transvaginal mesh, tape, or sling failure gets to the best possible attorneys, and the group is promising all of the suggested attorneys will be skilled plaintiffs attorneys, who are women. For more information a victim of a transvaginal mesh, tape, or sling failure can 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
  • Urinary problems
  • 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 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 these 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

Attachments