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US Drug Watchdog Now Urges Victims Of A Transvaginal Mesh, Tape Or Sling Failure To Call Them for the Names of Top Plaintiffs Attorneys–Who will all be Women

December 2, 2012

The US Drug Watchdog has dramatically grown their initiative focused on helping women recipients of a failed transvaginal mesh, tape, or sling, because they fear there could easily be thousands of US victims. According to the New York Times, “In 2010, about 185,000 women underwent procedures in which mesh was implanted vaginally to treat urinary incontinence.” Court records indicate a transvaginal mesh, tape, or bladder sling 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’s initiative is designed to assist any women in the US, who is a victim of a transvaginal mesh, or bladder sling failure, and the group will provide all women victims with the specific contacts of national caliber attorneys-who are all also women. For more information women, who are now victims of the Transvaginal Mesh Disaster are urged to call the US Drug Watchdog anytime at 8660714-6466. http://USDrugWatchdog.Com

(PRWEB) November 30, 2012

The US Drug Watchdog is now calling transvaginal mesh, tape, or sling failures a medical device disaster for thousands of US women, who must now suffer consequences that are almost beyond comprehension. The group is offering to help all US women, who are now victim’s of the transvaginal mesh disaster 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. 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.” The US Drug Watchdog has expanded their national initiative designed to help women recipients of transvaginal mesh, tape, or sling failure who are now severely injured by these types of medical products. For more information women, who are 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

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

  • Severe 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
  • 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, tape, or sling failures. 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 all women, who are 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)

For the original version on PRWeb visit: http://www.prweb.com/releases/prweb2012/11/prweb10138695.htm


Source: prweb



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