(PRWEB) January 15, 2013
The US Drug Watchdog has expanded their national initiative aimed at helping women, who are victims of a transvaginal mesh, tape, or bladder sling failure, because the vast majority of women victims they have talked to feel like the have been abandoned by their physicians, or surgeons on what was supposed to be a minimally evasive surgical procedure. The US Drug Watchdog says, "The FDA is now saying transvaginal mesh failures are 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 is offering to help all US women, who are now victim's of the transvaginal mesh, tape, or bladder sling failure get to the best possible attorneys, and because the damages, and costs are gender specific, and in many cases horrific, the group is promising the attorneys will all be women. For more information victims of a transvaginal mesh, tape, or bladder sling are urged to contact the US Drug Watchdog anytime at 866-714-6466, or contact the group via their web site at http://USDrugWatchdog.Com
The US Drug Watchdog is indicating symptoms of a vaginal mesh, tape, or bladder sling implant 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 the failures of a bladder sling, or transvaginal mesh, or tape. If you have a friend, or loved one who is a recipient of a transvaginal mesh, tape, or bladder sling 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 these 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 Multi District 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/2013/1/prweb10307836.htm.
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