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US Drug Watchdog Now Urges Any Woman Who Has A Transvaginal Mesh Failure Involved A Failed Corrective Surgery To Call Them For The Names of the Best Possible Lawyers

June 11, 2013

The US Drug Watchdog is now urging any recipient of a failed transvaginal mesh product, who has had a failed surgery to correct the mesh failure, or malfunction to call them for the names of national caliber lawyers who have a thorough understanding of transvaginal mesh devices, and are passionate about seeking justice for victims in a horrible situation. For more information victims of a transvaginal mesh failure involving severe medical complications, or an unsuccessful revision surgery are urged to contact the US Drug Watchdog anytime at 866-714-6466. http://USDrugWatchdog.Com

(PRWEB) June 11, 2013

The US Drug Watchdog says,”We are now urging any recipient who has a failed transvaginal mesh device, who has undergone a unsuccessful surgery to correct the failure, also known as revision surgery to call us for the names, and contacts of the most knowledgeable, and skilled transvaginal mesh lawyers in the nation, because we passionately believe these women really will need the best possible lawyers, if they are ever going to get meaningful justice.” According to court records, a transvaginal mesh failure occurs when the mesh fails to bind to a woman’s 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 is urging any woman, who has had the transvaginal mesh surgical procedure done, and now has developed severe medical complications, or has had a unsuccessful surgery to repair the failure to call them immediately 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

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, tape, or sling failure. We also need to emphasize this is a nationwide problem with women in every state including Florida, New York, Massachusetts, Maryland, New Jersey, Virginia, Ohio, Pennsylvania, Illinois, Missouri, Texas, New Mexico, Kansas, North Dakota, Colorado, Arizona, Utah, Montana, Idaho, California, and Washington. 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, tape, or sling failure victims get to the best possible attorneys, to ensure they get the best possible compensation for their ordeal.” 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)

For the original version on PRWeb visit: http://www.prweb.com/releases/prweb2013/6/prweb10757950.htm


Source: prweb



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