(PRWEB) December 17, 2012
The US Drug Watchdog is expanding their efforts to make certain all women recipients of transvaginal mesh, tape, or sling, who are now severely damaged by these types of medical products get to the best possible attorneys, and the group is promising the attorneys will all be women. 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 issues. The procedure to install a transvaginal mesh, tape, or sling was supposed to be minimally-invasive. The US Drug Watchdog is now saying, "According to court records the US 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 very passionaste about making certain all US women, who are 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. 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 implant, or sling failure may include:
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. If you have a friend, or loved one who is a recipient of a transvaginal mesh 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 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)
Read the full story at http://www.prweb.com/releases/2012/12/prweb10209600.htm.
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