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2013 Alleged Transvaginal Mesh Complications Lawsuits Update: Resource4thePeople Reports Defendants Ordered to Provide Testimony, Documents
Date:5/18/2013

ons to consumers inquiring about their legal options involving allegations of transvaginal mesh complications.

The South Dakota woman's lawsuit**** was the first to go to trial from among 2,100 transvaginal mesh lawsuits consolidated in New Jersey.

The Bloomberg News report said lawyers for the woman, Linda Gross, told jurors the defendants failed to warn the woman's surgeon of the risks of its Gynecare Prolift implant and fraudulently misled her about the risks.

According to the court file in the case, the 47-year-old Gross filed allegations complaining of constant pain and said she was forced to undergo 18 operations to repair abdominal injuries she suffered after having the device implanted to treat her pelvic organ prolapse.

Resource4thePeople spokesman Howell said consumers are often inquiring about whether it is too late to file a lawsuit on their behalf.

"The answer, in most cases, is no," said Howell. "Every case is different, however, and the easiest solution is for consumers to contact us for a free legal consultation."

Resource4thePeople also is recommending that women who have suffered health problems from transvaginal mesh products familiarize themselves with Food and Drug Administration warnings of “serious complications associated with transvaginal placement of surgical mesh for pelvic organ prolapse."*****

In the warning issued to health care professionals, the FDA cited recent medical literature which revealed that:

  •     Mesh used in transvaginal POP repair introduces risks not present in traditional non-mesh surgery for POP repair.
  •     Mesh placed abdominally for POP repair appears to result in lower rates of mesh complications compared to transvaginal POP surgery with mesh.
  •     There is no evidence that transvaginal repair to suppo
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Source: PRWeb
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