US Drug Watchdog Now Expands Their Transvaginal Mesh Initiative for All US Victims and They Are Offering the Names of the Best Possible Attorneys-Who Are also Women

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The US Drug Watchdog has expanded their very aggressive initiative designed to assist all victims of a transvaginal mesh, tape, or sling failure-because they are hearing from so many victims

(PRWEB) November 16, 2012

The US Drug Watchdog has expanded their national initiative designed to help victims of a transvaginal mesh, tape, or sling failure, who are now severely damaged by this type of medical product-because they see a great need for their unique service. 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." 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

The US Drug Watchdog is indicating symptoms of a transvaginal mesh, tape, or sling implant 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)
• Vaginal Bleeding
• Vaginal Infection
• Urinary problems (Non stop urinary tract infections-UTI's)
• 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 type product 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 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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