FDA Asks Manufacturers to Keep Their Transvaginal Mesh for POP Off the Market | |
The FDA has advised against a transvaginal mesh by Coloplast, and the manufacturer is compelled to keep the product off the market for the time being. The decision is based on a surveillance study of about 36 months. The Coloplast transvaginal mesh was for use in Pelvic Organ Prolapse (POP) | |
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Target State: All States Target City : New York City Last Update : Jan 24, 2025 1:16 AM Number of Views: 13 | Item Owner : medhealthreview Contact Email: Contact Phone: +1 702-213-6364 |
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