More Than 1,000 Victims Report Transvaginal Mesh Complications

October 10, 2011

According to the Food and Drug Administration (FDA), more than 1,000 victims in the last three years have reported complications with their transvaginal mesh devices. Typically, these devices were used in an attempt to repair POP and SUI. Tragically, however, in a number of these cases, the transvaginal mesh created more problems than it solved, including infection, pain, urinary problems, and a recurrence of prolapse. Although the FDA has yet to identify the specific contributing risk factors associated with transvaginal mesh complications, potential factors include mesh material, the size and shape of the transvaginal mesh, and the surgical technique used.

 

Fears Nachawati protects transvaginal mesh patients just like you! If you’ve been injured, it may be time to speak with our legal experts. We can help you understand your rights and determine the right way to move forward. For a free consultation, call us at 1.866.545.8364 or email mn@fnlawfirm.com. We’re ready to fight for you!

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