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FDA takes action to protect women’s health, orders manufacturers of surgical mesh intended for transvaginal repair of pelvic organ prolapse to stop selling all devices

07:49 EDT 16 Apr 2019 | FDA

FDA informs companies that the agency is not approving their PMA applications and that they will have to remove their products from the market

Original Article: FDA takes action to protect women’s health, orders manufacturers of surgical mesh intended for transvaginal repair of pelvic organ prolapse to stop selling all devices

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