The US Drug Watchdog is receiving daily complaints from victims of transvaginal mesh, tape, or sling failures related to the fact their doctor, or surgeon who implanted the device-will not return their phone calls?
(PRWEB) November 28, 2012
The US Drug Watchdog is now urging the US FDA step into what has turned into the atmospherics of the Wild West with respect to victims of a transvaginal mesh, tape, or sling failure. The US Drug Watchdog is receiving daily complaints from victims of transvaginal mesh, tape, or sling failures related to the fact their doctor, or surgeon who implanted the device-will not return their phone calls? Supposedly the procedure to install a transvaginal mesh, tape, or sling implant is minimally-invasive. 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 transvaginal mesh failure may need to have numerous corrective surgeries." The US Drug Watchdog is offering to help all US women, who are now victim's of a transvaginal mesh failure, tape, or sling failure and they are urging victims to call them for the names of best possible attorneys, and the group is promising the attorneys will all be women. For more information victims of the Transvaginal Mesh Disaster are urged to contact the US Drug Watchdog anytime at 866-714-646. http://USDrugWatchdog.Com
The US Drug Watchdog is indicating symptoms of a vaginal mesh, tape, or sling implant failure may include:
- Pain during sexual intercourse caused by erosion.
- Mesh erosion through the vagina (the mesh is actually protruding out of the vaginal wall)
- Vaginal Bleeding
- Vaginal Infection
- Urinary problems-constant 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 the transvaginal mesh, tape, or sling 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. 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, 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)