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US Drug Watchdog Now Urges Victims Of An Unsuccessful Transvaginal Mesh Revision Surgery Nationwide To Call Them For The Names Of The Best Lawyers-Who Will All Be Women
Date:4/30/2013

(PRWEB) April 30, 2013

The US Drug Watchdog is now very focused on helping all US women, who are victims of a transvaginal mesh failure that includes a unsuccessful revision surgery. Because of the sensitive nature of a transvaginal mesh failure the US Drug Watchdog is offering failure victims the names of the best possible attorneys, and because the damages are so gender specific, and so personal, the group is promising the attorneys will all be women. The US Drug Watchdog is saying, "We are talking to victims multiple times per week who have had an unsuccessful revision surgery, and these women are being told by their doctors there is nothing else that can be done? We say baloney. If you are a victim of a severe transvaginal mesh failure, or a unsuccessful revision surgery call us and we will give you the names, and contacts of national caliber attorneys who are all women, and extremely good at what they do." According to the US FDA, transvaginal mesh, tape, or sling failures are causing complications in patients such as erosion, or serious infections. Women who experience transvaginal mesh failure may need to have numerous corrective surgeries, IV therapy, blood transfusions and drainage of hematomas or abscesses. 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.

The US Drug Watchdog is indicating symptoms of a transvaginal mesh implant failure may include:

  • Mesh erosion through the vagina (the mesh is actually protruding out of the vaginal wall)
  • Vaginal Bleeding
  • Vaginal Infection
  • Urinary problems ( Non stop UTI's)
  • 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 failure. Transvaginal mesh failure victims are not just isolated to one state like California, or New York. 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." For more information please call the US Drug Watchdog anytime at 866-714-6466. 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/2013/4/prweb10674059.htm.


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1. US Drug Watchdog Now Urges Victims Of A Severe Transvaginal Mesh Implant Failure To Call Them For The Names Of National Caliber Women Attorneys-Get Compensated
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4. US Drug Watchdog Now Urges All Transvaginal Mesh Failure Victims Of A Unsuccessful Revision Surgery Or Erosion To Call Them For The Names Top Attorneys-Who Are All Women
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