Transvaginal Mesh Implant

The following complications have been reported as a result of the Transvaginal pelvic organ prolapse (POP) mesh implant procedure:

  • Mesh erosion
  • Pelvic pain
  • Infection
  • Bleeding
  • Urinary leakage
  • Pain during sexual intercourse
  • Recurrence of prolapse
  • Organ perforation

FDA Warnings About Transvaginal Mesh

On July 13, 2011, the FDA issued a Safety Communication titled, "UPDATE on Serious Complications Associated with Transvaginal Placement of Surgical Mesh for Pelvic Organ Prolapse."

Click here to view the entire FDA warning.

The FDA communication noted that even though there was an increased risk of these serious complications, there was no corresponding clinical evidence of greater benefit, such as an improved quality of life. Furthermore, the FDA reported that these complications were not rare.

If you are a woman who has had surgery to correct pelvic prolapse or urinary incontinence and were told a transvaginal mesh implant or bladder sling implant was used and then you developed serious complications after surgery, you may have a claim.

Following surgery, some women have experienced bowel or bladder perforation or other serious injuries to the bladder. You may have had additional surgery to remove the mesh implant.

If you have experienced serious problems following surgery from a mesh implant, call Goldberg Attorneys, 800.600.6014, for a free, confidential consultation.


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