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How Much Do You Know About Your Transvaginal Mesh Operation?

February 13, 2012

If you’d like to think that the risk of transvaginal mesh complications is remote, you can, but the Food and Drug Administration (FDA) will disagree with you. In fact, the FDA has taken the unusual step of writing in bold text that serious complications associated with surgical transvaginal repairs of pelvic organ prolapse (POP) were “not rare.”


Pelvic organ prolapse and stress urinary incontinence (SUI) are not uncommon ailments, particularly for women who have recently given birth or experienced menopause. However, reports of transvaginal mesh complications are common. In simple terms, the tragic reality is that the medical device community has manufactured a product in transvaginal mesh devices that exposes patients to serious potential injury.


Have you suffered unexpected pain and discomfort as a result of your transvaginal mesh operation? That’s not the way surgery is supposed to be. It may be time to talk to the legal experts at Fears Nachawati to find out if you have a viable claim under the law. Based on the fail rate of transvaginal mesh operations, many patients have valid causes of action. Find out everything you need to know by contacting us today. For your free consultation, call us at 1.866.545.8364 or email


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