The Hollis Law Firm P.A.
5100 West 95th Street
Prairie Village, KS 66207
Serious side effects have been linked to Urogynecologic Surgical Mesh implants used to repair Stress Urinary Incontinence (SUI) and Pelvic Organ Prolapse (POP) in women.
Complications include:
Some women have experienced painful mesh erosion, in which the skin splits and the mesh protrudes, and contraction of the mesh, leading to vaginal shrinkage.
In 2008, the Food & Drug Administration (FDA) warned doctors that transvaginal placement of surgical mesh products used to reinforce weakened tissues in women generated more than 1,000 reports of adverse events. The FDA has since issued an update to that warning; between 2008 and 2010, nearly 3000 reports were made to the FDA regarding problems with urogynecologic surgical meshes. The FDA recommends that women talk with their surgeons about potential complications.
SUI and POP are commonly found in women, especially after childbirth, and are a result of a weakening of the muscles of the pelvic floor. Urogynecologic Surgical Mesh is a plastic screen implanted by a surgeon the through an incision made in the vaginal wall to help support the weakened muscles.
Urogynecologic Surgical Mesh was first used to treat SUI 1996, and then to treat POP in 2002. If you have had surgery to correct SUI or POP (which includes cystocele, procidentia, rectocele, apical prolapse, or enterocele) after these dates, contact your doctor, who will have records that indicate whether mesh was used.
If you are having symptoms or complications such as unusual bleeding, pain, or discharge you should consult your doctor as soon as possible.
We cannot answer that question without speaking to you personally. No two people are the same. Your injury might be different from that of another individual.
If you or a loved one developed serious complications after vaginal mesh implant surgery, you may be entitled to compensation. Call today at (800) 701-3672 and speak to one of our trained team members, or complete a Quick Case Review, to receive a FREE case evaluation.
References:
1. Food and Drug Administration, Center for Devices and Radiological Health, Urogynecologic Surgical Mesh: Update on the Safety and Effectiveness of Transvaginal Placement for Pelvic Organ Prolapse, July 13, 2011; available at: http://www.fda.gov/downloads/MedicalDevices/Safety/AlertsandNotices/UCM262760.pdf
2. Christine Mai Duc, FDA Reevaluating Vaginal Mesh Implants, Los Angeles Times, July 13, 2011, available at: http://www.latimes.com/health/sc-dc-0714-fda-mesh-20110714,0,3218985.story
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