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Why Did OB/GYN Doctors Testify Before the FDA about Transvaginal Mesh?

About this time last year, numerous OB/GYN doctors from across the country testified before the Food and Drug Administration (FDA), the governmental agency responsible for assuring that the drugs Americans take are safe. The topic of their testimony was the extent to which transvaginal mesh procedures may injure patients and whether the risk is so high that these medical devices should be pulled from the market. In short, many health experts and consumer advocates believe the answer is yes.


Are you one of the thousands of American women who have experienced adverse affects as a result of your transvaginal mesh operation? Whether you’re recovering from a flawed pelvic organ prolapse (POP) or stress urinary incontinence (SUI) procedure, the fact of the matter is that justice and appropriate compensation may be within your grasp. Don’t let your rights become stale because were afraid to ask a few questions.


The attorneys at the Dallas law firm of Fears Nachawati have years of experience fighting for victims just like you. We know what it takes to present your case, and we have the resources to see your claims litigated to their fullest appropriate extent. Find out how we can help you on the road to recovery. For your free consultation, call us at 1.866.545.8364 or email We’re ready to fight for you!

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Why Did OB/GYN Doctors Testify Before the FDA about Transvaginal Mesh?