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US Drug Watchdog Now Urges Transvaginal Mesh, Tape, or Bladder Sling Failure Victims To Call Them For the Names of Top Plaintiffs Women Attorneys--Erosion Is Not Normal
Date:1/24/2013

(PRWEB) January 24, 2013

The US Drug Watchdog is urging women, who are recipients of a transvaginal mesh, tape, or bladder sling, and have been told erosion, and or the mesh poking through the vaginal wall is quote, "Normal." to call them for the names of national caliber attorneys who are all also women. The group is offering to help all US women, who are now victims of a transvaginal mesh, tape, or bladder sling failure get to the best possible national caliber attorneys who are all also women, because the damages such as erosion are so gender specific. As a background, 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." For more information women, who are victims of a transvaginal mesh, tape, or bladder sling failure are urged to contact the US Drug Watchdog anytime at 866-714-6466, or contact the group via their web site at http://USDrugWatchdog.Com

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

  • Pain during sexual intercourse caused by erosion
  • No possibility of sexual intercourse
  • Mesh erosion through the vagina (the mesh is actually protruding out of the vaginal wall)
  • Vaginal Bleeding
  • Vaginal Infection
  • Urinary problems
  • 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 the transvaginal mesh product failures. If you have a friend, or loved one who is a recipient of a transvaginal mesh, tape, or bladder 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 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 & Johnsons Ethicon, Inc. (MDL No. 2327)

Read the full story at http://www.prweb.com/releases/2013/1/prweb10330933.htm.


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