(PRWEB) February 20, 2013
The US Drug Watchdog is now urging women who either have a transvaginal mesh, tape, or bladder sling product that has failed, or a woman who has gone through an unsuccessful surgery to repair a transvaginal mesh product failure to call them for the names of the best possible attorneys, who are also women, especially if the victims doctor is ignoring them, or telling them nothing else can be done. The US FDA is now saying transvaginal mesh, tape, or sling failures are causing complications in patients such as erosion and infection. Women who experience transvaginal mesh failure may need to have numerous corrective surgeries, IV therapy, blood transfusions and drainage of hematomas or abscesses." The US Drug Watchdog has dramatically expanded their national initiative designed to help women recipients of transvaginal mesh, tape, or a sling, who are now severely injured by these types of medical products, because. 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, or contact the group via their web site at http://USDrugWatchdog.Com
The US Drug Watchdog is saying, "What has us so concerned at this moment is many of women we talk to, who are having to live with the daily consequences of a transvaginal mesh, tape, or bladder sling failure are being told by their doctor, or surgeon there is nothing more that can be done, or the doctor is not even returning the victims phone calls, or e-mails? We really do want to help all of these women, and we don't care if they are in California, New York, Ohio, Florida, Alaska, Texas, or any other US state." http://USDrugWatchdog.Com
The US Drug Watchdog is now saying, "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, and or non stop UTI's, organ perforation, hardening of the vaginal mesh, injury to nearby organs, and or severe pelvic pain." 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/2013/2/prweb10410452.htm.
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