(PRWEB) January 16, 2013
The US Drug Watchdog says, "We are extremely motivated to get all women who are victims of a transvaginal mesh, tape, or bladder sling failure identified to the best possible attorneys, who are all also women, because we know the medical complications associated with a failure can be horrific, and because we know many of the women victims we talk to have been ignored by their physician, or surgeon, In one instance we heard from a woman who had transvaginal mesh poking out of her vaginal wall, and her physician took what appeared to be fingernail clippers, clipped the piece of mesh protruding out of the vaginal wall, gave her some cream, and said, quote you are good to go. We hear this same type of story every few days." As a background, according to court records a transvaginal mesh 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." Erosion may result in extreme pain, infection, and bleeding. The US Drug Watchdog has expanded their very aggressive initiative designed to assist all women in the United States, who are victims of a transvaginal mesh, tape, or bladder sling failure, because they believe there is a very great need for this service. The group is urging any woman, who has had the transvaginal mesh type product surgical procedure done, and now has developed severe medical complications to call them anytime at 866-714-6466. As part of their initiative the US Drug Watchdog is offering to send all US women, who are victims of a transvaginal mesh, tape, or bladder sling failure to national caliber attorneys-who are all also women. 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 transvaginal mesh, tape, or bladder sling failures. 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 these transvaginal mesh, tape, or bladder 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/2013/1/prweb10308239.htm.
Copyright©2012 Vocus, Inc.
All rights reserved