US Drug Watchdog Now Urges Transvaginal Mesh Failure Victims To Call Them For The Names of The Best Possible Women Attorneys If they Had A Unsuccessful Repair Surgery

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The US Drug Watchdog says, "We are now urging women who underwent an unsuccessful surgery to repair a transvaginal mesh failure to call us at 866-714-6466, for the names, and contact information for leading national caliber lawyers, who are all women, and who are also very passionate about obtaining justice for these specific types of victims." http://USDrugWatchdog.Com

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The US Drug Watchdog is now urging a victim of a transvaginal mesh failure, who also has had a unsuccessful revision surgery to repair the problem to call them for the names, and contact information for national caliber lawyers, who are all women

The US Drug Watchdog is urging a victim of a transvaginal mesh failure, who also has had an unsuccessful revision surgery to repair the problem to call them for the names, and contact information for national caliber lawyers, who are all women, and who share the group's passion about compensation for victims. 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." The US Drug Watchdog is offering to help all US women, who underwent a unsuccessful surgery to repair a failed transvaginal mesh product, and the group is promising because the damages are so gender specific, the lawyers they suggest will all be women. For more information victims of a transvaginal mesh failure who have developed very severe medical complications are urged to contact the US Drug Watchdog anytime at 866-714-646.

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

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. We cannot emphasize enough that there are victims in every state from the largest by population like California, New York, Texas, and Florida, to the smallest by population such as Maine, Wyoming, South Dakota, or Alaska. 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 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)

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M Thomas Martin
Americas Watchdog
866-714-6466
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