Between 1992 and 2010, the FDA approved 85 surgical mesh devices to treat pelvic organ prolapse, and in just the last year more than 300,000 American women underwent surgical procedures to repair prolapsed organs, according to FDA reports. More than a quarter of these operations used transvaginal mesh. For a significant number of these women, the high-risk associated with these devices caused a variety of pelvic-related medical problems.
Fears Nachawati is leading the fight to protect victims of this dangerous medical device. For hundreds of women annually, transvaginal mesh causes considerable harm to their bodies and their futures. If you or a loved one have suffered complications from these medical devices, you need to let us know. For your free consultation, call us at 1.866.545.8364 or email mn@fnlawfirm.com. We’re ready to fight for you!