Check with seller FDA Asks Manufacturers New York City
- Location: New York City, New York City, New York, USA
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)
For more details please visit our website : https://www.medhealthreview.com/2022/10/21/fda-asks-manufacturers-to-keep-their-transvaginal-mesh-for-pop-off-the-market/
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