(PRWEB) April 11, 2013
The US Drug Watchdog says, "Transvaginal mesh failures are the worst medical device failures we have ever heard of, because the complications related to a transvaginal mesh failure can be so severe, and complex, especially if we are talking about erosion, or a revision surgery that failed. Based on the severity of these gender specific types of damages we will make certain victims get to national caliber attorneys-who are all also women." 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." The US Drug Watchdog is urging any woman, who has had the transvaginal mesh surgical procedure done, and now has developed severe medical complications to call them immediately at 866-714-6466.
The US Drug Watchdog is indicating symptoms of a transvaginal 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 a transvaginal mesh, tape, or sling failure. The issue of transvaginal mesh failures, and or severe complications such as erosion are not getting much national press, outside of a few articles in the New York times, but this really is a national problem with victims in all 50 US states. 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 these 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)