Da Vinci Xi Tenaculum Forceps And Retractor
Da Vinci Xi Tenaculum Forceps and Retractor Recall Da Vinci Xi Tenaculum Forceps and Retractor instruments are being recalled across Canada due to a performance issue. This recall affects medical devices used in surgical procedures. The FDA has classified this as a Class I recall, the most serious category.
- Product
- Da Vinci Xi Tenaculum Forceps and Retractor
- Reason
- Performance
- Classification
- Class I
- Category
- drug recall
- Country
- Canada
- Agency
- HC-DEVICES
- Recall date
- 2025-02-04
- Status
- Ongoing
- Distribution
- Canada-wide
Official recall notice from HC-DEVICES
Recall details on Nibble Recalls: https://trynibble.app/recalls/cc67c19f-acc6-41c6-84d3-0d520583bede