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US Drug Watchdog Now Urges Transvaginal Mesh Failure Victims With A Failed Revision Surgery to Call Them for the Names of the Best Possible Women Attorneys
Date:4/12/2013

(PRWEB) April 12, 2013

The US Drug Watchdog is receiving daily complaints from victims of a transvaginal mesh failure, typically related to the fact their doctor, or surgeon who implanted the device-will not return their phone calls? Supposedly the procedure to install a transvaginal mesh, tape, or sling implant was going to be minimally-invasive? The US Drug Watchdog says, "The 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." The US Drug Watchdog is offering to help all US women, who are now victim's of a transvaginal mesh failure, especially if the failure involves erosion, or if the victim has had a unsuccessful revision, or repair surgery, and they are urging victims to call them for the names of best possible attorneys, and the group is promising the attorneys will all be women, because the damages are so gender specific. For more information victims of a transvaginal mesh failure are urged to contact the US Drug Watchdog anytime at 866-714-646.

The US Drug Watchdog is indicating symptoms of a vaginal mesh, tape, or sling 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-constant UTI's
  • Organ perforation
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 failures. This is a nationwide issue involving women in the biggest states like California, New York, Florida, and Texas, to the smallest by population such as Maine, Alaska, South Dakota, or Wyoming. If you have a friend, or loved one who is a recipient of a transvaginal mesh type 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 these 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)

Read the full story at http://www.prweb.com/releases/2013/4/prweb10607603.htm.


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