US Drug Watchdog Now Urges Transvaginal Mesh, Tape, or Sling Failure Victims to Call Them for the Names of the Best Possible Women Attorneys & They Urge an FDA Response

The US Drug Watchdog says, "We are now calling transvaginal mesh failure issues the absolute worst mess we have ever seen for women, and the damages are literally beyond comprehension. We are also talking about a potentially huge number of US women. 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. Our question now is pretty basic---where is the US FDA, and the FDA recalls?" According to court records a 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 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 is receiving daily complaints from victims of transvaginal mesh, tape, or sling failures related to the fact their doctor, or surgeon who implanted the device-will not return their phone calls?

(PRWEB) November 28, 2012

The US Drug Watchdog is now urging the US FDA step into what has turned into the atmospherics of the Wild West with respect to victims of a transvaginal mesh, tape, or sling failure. The US Drug Watchdog is receiving daily complaints from victims of transvaginal mesh, tape, or sling failures related to the fact their doctor, or surgeon who implanted the device-will not return their phone calls? Supposedly the procedure to install a transvaginal mesh, tape, or sling implant is minimally-invasive. The US Drug Watchdog 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 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 failure, tape, or sling failure and they are urging victims to call them for the names of best possible attorneys, and the group is promising the attorneys will all be women. For more information victims of the Transvaginal Mesh Disaster are urged to contact the US Drug Watchdog anytime at 866-714-646. http://USDrugWatchdog.Com

The US Drug Watchdog is indicating symptoms of a vaginal 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-constant 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 the transvaginal mesh, tape, or sling failures. If you have a friend, or loved one who is a recipient of a transvaginal mesh 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 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

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