Transvaginal Mesh Surgery for Pelvic Organ Prolapse
In April 2019, the Food and Drug Administration (FDA) ordered that all makers of vaginal mesh for transvaginal repair of pelvic organ prolapse to stop producing and distributing this product immediately. Every year, thousands of women undergo surgery to repair their pelvic floor. However, the FDA has judged that makers of these devices "have not demonstrated reasonable assurance of safety and effectiveness." Therefore, the FDA is taking action to protect the health of these women across the United States.