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Vaginal Mesh Lawsuit Filed by Wright & Schulte Claims Nebraska Woman Sustained Painful Injuries Allegedly Due to Defective Vaginal Mesh Implants
Date:4/6/2013

, mesh erosion through the vaginal lining, an increased risk of infection, puncturing of the blood vessels/bowels/bladder and recurrence of SUI. [http://www.fda.gov/downloads/MedicalDevices/Safety/AlertsandNotices/UCM262760.pdf

FDA Warning Concerning Vaginal Mesh Risks
Following a review of more than 100 studies on bladder mesh slings, in 2011, the Food and Drug Administration (FDA) announced that transvaginal mesh complications more common than manufacturers initially warned and that, in some cases, vaginal mesh implants were no more effective at treating POP or SUI than traditional surgeries. Specifically, the FDA found that approximately 10 percent of patients who had transvaginal mesh implants have developed or would develop serious injuries that would require corrective surgery and may be even the removal of the vaginal mesh within 12 months of implantation. In some of the worst cases, women reportedly needed more than one revision surgery to try to correct the damage caused by bladder mesh slings.

The FDA’s 2011 warning also informed the public that vaginal mesh devices had greater risks of complications than traditional surgery for treating POP and SUI and that vaginal mesh implants may not even be sufficient at alleviating the symptoms of prolapse. [http://www.fda.gov/downloads/MedicalDevices/Safety/AlertsandNotices/UCM262760.pdf

About Wright & Schulte LLC And Filing A Vaginal Mesh Lawsuit
Wright & Schulte LLC, an experienced personal injury firm, is dedicated to the belief that America’s legal system should work for the people. Every day, the attorneys of Wright & Schulte LLC stand up for the rights of people who have been injured or wronged and fight tir
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3. TransVaginal Mesh Lawsuit Filed on Behalf of a Georgia Woman Seriously Injured Allegedly Due to Defective TransVaginal Mesh Implants, Reports Wright & Schulte
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