(PRWEB) June 10, 2013
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 a transvaginal mesh failure may need to have numerous corrective surgeries." According to court records, "Transvaginal mesh, tape or bladder sling 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 woman in the US, who is a victim of severe medical complications such as erosion, because of a transvaginal mesh failure, and they are urging victims to contact them anytime at 866-714-6466 for the names, and contacts of national caliber lawyers who are passionate about helping victims coast to coast.
The US Drug Watchdog is indicating symptoms of a vaginal mesh, tape, or 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 failures. If you have a friend, or loved one who is a recipient of a transvaginal mesh type product that has already failed or is showing symptoms of a failure, please have them call us at 866-714-6466, and we want emphasize this is a national initiative focused on helping women in California, New York, Florida, Texas, Ohio, Kansas, Idaho, Tennessee, Oklahoma, Maine, Massachusetts, Oregon, Colorado, New Mexico, and every other state. We want to make certain these transvaginal mesh failure victims get to the best possible attorneys, to ensure they get the best possible compensation for their ordeal." 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/2013/6/prweb10791622.htm.
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