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US Drug Watchdog Now Urges Transvaginal Mesh Product Failure Victims Who Have Had A Unsuccessful Revision Surgery To Call Them For The Names Of The Best Women Attorneys
Date:1/23/2013

(PRWEB) January 23, 2013

The US Drug Watchdog is now urging victims of a transvaginal mesh, tape, or bladder sling failure to call them for the names of national caliber women attorneys, who have significant knowledge related to these types of medical product failures, and because the damages are so gender specific. At the same time the group would like to hear from women who had a failed repair, or a unsuccessful transvaginal mesh product revision surgery, again with the goal being these victims get to top national women attorneys. As a background, according to court records, transvaginal mesh products were designed for women, who were suffering from pelvic organ prolapse, and stress urinary incontinence. The procedure to install a transvaginal mesh was supposed to be minimally-invasive. The US Drug Watchdog 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." For more information victims of a transvaginal mesh, tape, or bladder sling failure 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 transvaginal mesh product 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)
  • 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
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