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FDA takes action to protect women's health

from FDA

The U.S. Food and Drug Administration ordered on April 16 the manufacturers of all remaining surgical mesh products indicated for the transvaginal repair of pelvic organ prolapse to stop selling and distributing their products in the U.S. immediately. The order is the latest in a series of escalating safety actions related to protecting the health of the thousands of women each year who undergo surgery transvaginally to repair POP. more


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