Mesh implantation can lead to a serious decline in quality of life.

On October 20, 2008, the FDA issued a Public Health Notification about serious complications associated with transvaginal placement of surgical mesh to repair pelvic organ prolapse and stress urinary incontinence.

Transvaginal Surgical Mesh

FDA: “Transvaginal Mesh Carries An Increased Rate of Side Effects”
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The FDA has received thousands of reports of complications from women injured by transvaginal mesh. Women and their families have filed more than 90,000 federal lawsuits against the manufacturers of these products.


    • The FDA has issued a statement warning about serious complications associated with the surgical mesh.
    • Transvaginal Mesh Surgery complications are linked to several manufacturers, which may qualify you or a loved one for a claim.
  • The time to file a Transvaginal Mesh lawsuit is NOW!

According to the FDA’s notification, “Specific characteristics of patients at increased risk for complications have not been determined. Contributing factors may include the overall health of the patient, the mesh material, the size and shape of the mesh, the surgical technique used, concomitant procedures undertaken (e.g. hysterectomy), and possibly estrogen status.”

Unfortunately, complications from the implantation of a Bard Avaulta or other mesh can lead to a serious decline in the patient’s quality of life. At Reyes Browne Reilley Law Firm, we have worked with many individuals and families who have been injured by dangerous products such as the Bard Avaulta Mesh.

At Reyes Browne Reilley Law Firm, you, as our client, will always come first.

Transvaginal Mesh Lawsuit (Vaginal Mesh Implant or Trans Vaginal Mesh) Free Consultation:

If you or a loved one has suffered injury as a result of the implantation of this device, please contact our offices at 214-526-7900 or fill out our Case Review Contact Form on this page, so we can help you.