(PRWEB) May 03, 2013
The US Drug Watchdog is now urging a victim of a transvaginal mesh failure involving erosion, unsuccessful revision surgery, or organ perforation to call them immediately for the names of national caliber women lawyers, who are also deeply involved in the national litigation involving these types of medical devices. According to court records, "A transvaginal 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." The US Drug Watchdog's initiative is designed to assist any women in the US, who is a victim of a transvaginal mesh failure involving erosion, or organ perforation, and the group will provide all victims with the specific contacts of national caliber attorneys-who are all women, because the damages are so gender specific. For more information please call the US Drug Watchdog at 866-714-6466.
According to the New York Times, "In 2010 185,000 US women were involved in a surgical procedure involving a transvaginal mesh product. That was just one year." The US Drug Watchdog says, "Transvaginal mesh failures are occurring in all US states. One of our new big worries is for victims who live in rural states like Iowa, Maine, Kansas, Oklahoma, Wyoming, Montana, Idaho, or Alaska. The question is will there be surgeons in these states skilled enough to actually repair a transvaginal mesh failure, or will these victims have to travel to California, New York, Washington, Ohio, Illinois, Massachusetts, or Florida to get meaningful treatment. Who pays for this?" http://USDrugWatchdog.Com
The US Drug Watchdog is indicating symptoms of a transvaginal mesh 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 a transvaginal mesh failure. If you have a friend, or loved one who is a recipient of a transvaginal mesh, tape 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 women, who are 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/2013/5/prweb10693607.htm.
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