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US Drug Watchdog Now Expands Their Efforts to Help Victims of a Transvaginal Mesh Product Failure with a Focus on the Best Women Attorneys and Financial Compensation

(PRWEB) January 03, 2013

The US Drug Watchdog is going to dramatically expand their initiatives focused on transvaginal mesh, tape, and bladder sling failures in 2013, because the group believes there is a great need for this service. Aside from weekday press releases, the group intends to coordinate a social media campaign, as well as make certain any victim they talk to has instant access to national caliber attorneys, who are all women. The goal is financial compensation for victims. According to court records transvaginal mesh, tape, or sling 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 bladder sling, who are now severely injured by these types of medical products-because their doctors in many instances are telling the woman vaginal bleeding, or erosion is quote, normal. 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 bladder 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 transvaginal mesh, tape, or bladder sling failure. 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 all women, who are transvaginal mesh, tape, or bladder 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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Source: PRWeb
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