US Drug Watchdog Now Urges Victims of a Transvaginal Mesh, Tape, or Sling Failure to Call Them for the Names and Contacts of the Best Women Attorneys-For Help & Support

The US Drug Watchdog says, "We could have thousands, or even tens of thousands of women in the United States, who are in unspeakable pain, or they have been damaged beyond comprehension, because they got sold a bill of goods. According to court records the surgical procedure to get a transvaginal mesh product was supposed to be minimally invasive. Now these women might have to have numerous corrective surgeries. We are outraged." Transvaginal mesh failure occurs when the mesh fails to bind to the 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 has begun a very aggressive initiative designed to assist women in the United States, in what they are referring to as the Transvaginal Mesh Disaster. The group is urging any woman, who has had the transvaginal mesh surgical procedure done, and now has developed severe complications to call them anytime at 866-714-6466. As part of its initiative the US Drug Watchdog is offering to send all US women, who are victims of this Transvaginal Mesh Disaster to national caliber attorneys-who are all women. http://USDrugWatchdog.Com

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Quote startAccording to court records the surgical procedure to get a transvaginal mesh product was supposed to be minimally invasive. Now these women might have to have numerous corrective surgeries. We are outragedQuote end

(PRWEB) October 18, 2012

The US Drug Watchdog now says, "A transvaginal mesh product failure victim's has been damaged beyond anything we could ever imagine. You could not make this nightmare up. The FDA is now saying transvaginal mesh failures are causing complications in patients such as erosion and infection. Patients who experience transvaginal mesh failure have needed corrective surgeries, IV therapy, blood transfusions and drainage of hematomas or abscesses." The US Drug Watchdog has launched an aggressive initiative designed to help victims of a transvaginal mesh product failure, who are now severely damaged. Transvaginal mesh, tape, or slings were designed for women, who were suffering from pelvic organ prolapse and stress urinary incontinence. The US Drug Watchdog is offering to help any victim of a transvaginal mesh failure get to the best possible attorneys, and the group is promising the attorneys will all be women. For more information 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 says 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." http://USDrugWatchdog.Com

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 Disaster. If you have a friend, or loved one who is a recipient of a Transvaginal Mesh 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 Disaster 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

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Contact

  • M Thomas Martin
    Americas Watchdog
    866-714-6466
    Email

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