What makes this effort unique is this the group will only offer the names of national caliber attorneys-who are also women-to a victim of a transvaginal mesh, tape, or sling failure
(PRWEB) October 16, 2012
The US Drug Watchdog has created a very aggressive national initiative focused on identifying all US women, who are victims of a transvaginal mesh, tape, or sling failure. What makes this effort unique is the group will only offer the names of national caliber attorneys-who are also women-to a victim of a transvaginal mesh, tape, or sling failure. No group or organization in the United States offers a service like this. According to the New York Times, Transvaginal mesh products were designed for women, who were suffering from pelvic organ prolapse, or stress urinary incontinence, and the procedure to install a transvaginal was supposed to be minimally-invasive." The US 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, blood transfusions and drainage of hematomas or abscesses." The US Drug Watchdog has created their national initiative designed to help women recipients of transvaginal mesh, tape, or sling, who are now severely injured by these types of medical products-because they fear there is a great need for this very unique service. For more information women, who are victims of a transvaginal mesh 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/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
- 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 a transvaginal mesh product. Because a transvaginal mesh, or sling failure is such a sensitive topic we fear the national news media will never adequately cover this vital news story. If you have a friend, or loved one who is a recipient of a transvaginal mesh, or sling 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 women, who are 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)
