The US Drug Watchdog is now calling transvaginal mesh, tape, or sling failures a medical device disaster for thousands of US women, who must now suffer consequences that are almost beyond comprehension
(PRWEB) November 30, 2012
The US Drug Watchdog is now calling transvaginal mesh, tape, or sling failures a medical device disaster for thousands of US women, who must now suffer consequences that are almost beyond comprehension. The group is offering to help all US women, who are now victim's of the transvaginal mesh disaster get to the best possible attorneys, and the group is promising the attorneys will all be women. No other Group is offering a service like this. Supposedly transvaginal mesh products were designed for women, who were suffering from pelvic organ prolapse, and or stress urinary incontinence. According to the US FDA the procedure to install a transvaginal was supposed to be minimally-invasive. The US Drug Watchdog now says, "The FDA is now saying transvaginal mesh failures is 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 has expanded their national initiative designed to help women recipients of transvaginal mesh, tape, or sling failure who are now severely injured by these types of medical products. For more information women, who are victims of a transvaginal mesh, tape, or sling failure are urged to contact the US Drug Watchdog anytime at 866-714-6466. http://USDrugWatchdog.Com
The US Drug Watchdog is indicating symptoms of a transvaginal mesh, tape, or sling implant failure may include:
- Severe 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
- Organ perforation
- Hardening of the vaginal mesh
- Injury to nearby organs
- Severe Pelvic Pain
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, 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 all women, who are 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)
