US Drug Watchdog Now Urges All Women Who Are US Victims Of A Transvaginal Mesh, Tape or Sling Failure To Call Them For the Names of the Best Possible Women Attorneys

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The US Drug Watchdog is now urging women who are victims of a transvaginal mesh, tape, or sling failure to call them for the names of the best possible attorneys-who will all be women. Supposedly transvaginal mesh type products were designed for women, who were suffering from pelvic organ prolapse, and or stress urinary incontinence. According to court records the procedure to install a transvaginal mesh, tape, or sling 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, tape, or sling 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

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Many of the women we are talking to cannot get a return call from their doctor, or they are being told erosion is not that big of a deal. Erosion is a piece of the transvaginal mesh poking through a woman's vaginal wall, and it is a very big deal

The US Drug Watchdog is aggressively expanding their initiative focused on helping women recipients of a failed transvaginal mesh, tape, or a sling to all women recipients, who have suffered a failure. The group says, "Many of the women we are talking to cannot get a return call from their doctor, or they are being told erosion is not that big of a deal. Erosion is a piece of the transvaginal mesh poking through a woman's vaginal wall, and it is a very big deal.This literally is the absolute worst medical device failure we have ever heard of because the complications are so severe. We are incredibly passionate about making certain these women victims get to the highest caliber attorneys-who are all women." 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 has now developed severe complications to call them immediately at 866-714-6466. http://USDrugWatchdog.Com

The US Drug Watchdog is indicating symptoms of a transvaginal mesh or sling implant failure may include:

  • Extreme 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 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)

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M Thomas Martin
Americas Watchdog
866-714-6466
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