(PRWEB) June 06, 2013
The US Drug Watchdog is urging any transvaginal mesh implant recipient who now has developed a severe medical complication known as erosion to call them for the names, and contacts of the nation's leading transvaginal mesh lawyers, because these types of complications may require costly corrective surgeries, so the victim's attorneys have to be extremely capable to ensure justice is actually done. 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." The US Drug Watchdog is urging any woman, who has had the transvaginal mesh surgical procedure done, and has now developed severe medical complications, such as erosion to call them immediately at 866-714-6466.
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, tape, or sling failure. We really need to emphasize this is a nationwide problem involving women in all US states including Massachusetts, New York, New Jersey, North Carolina, Florida, Georgia, Kentucky, Ohio, Indiana, Missouri, Texas, Oklahoma, Nebraska, Colorado, California, Montana, Idaho, Washington, and Alaska. If you have a friend, or loved one who is a recipient of a transvaginal mesh, tape, or 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 sling 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/prweb10757835.htm.
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