The women victims we refer to have a medical condition called erosion, or they have already had at least one unsuccessful surgery to repair, or remove the transvaginal mesh product
(PRWEB) May 06, 2013
The US Drug Watchdog says, "The only way we could describe a failure of a transvaginal mesh implant at least for some women is catastrophic. The women victims we refer to have a medical condition called erosion, or they have already had at least one unsuccessful surgery to repair, or remove the transvaginal mesh product. We are urging any woman, who has had the transvaginal mesh surgical procedure done, and now has developed severe medical complications to call us anytime at 866-714-6466. As part of our initiative we are offering to send all US women, who are victims of a transvaginal mesh failure to national caliber attorneys-who are all women, because the damages are so gender specific, complicated, and severe." 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 indicating symptoms of a transvaginal mesh implant failure may include:
- Mesh erosion through the vagina (the mesh is actually protruding out of the vaginal wall)
- Vaginal Bleeding
- Vaginal Infection
- Urinary problems (non-stop UTI's)
- Organ perforation
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. Transvaginal mesh victims are in every US state from the biggest like California, New York, Texas, or Florida, to the smallest by population like Maine, South Dakota, Montana, or Wyoming, and every other state. 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. We want to make certain all 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)