Da Vinci Xi And X 12-8 Mm Cannula Reducer
Da Vinci Xi And X 12-8 Mm Cannula Reducer Recall Da Vinci Xi and X 12-8 mm cannula reducers are being recalled across Canada due to a quality issue. This product is used in surgical systems. The FDA has classified this as a Class I recall, which is the most serious category.
- Product
- Da Vinci Xi And X 12-8 Mm Cannula Reducer
- Reason
- Quality
- Classification
- Class I
- Category
- drug recall
- Country
- Canada
- Agency
- HC-DEVICES
- Recall date
- 2022-01-24
- Status
- Ongoing
- Distribution
- Canada-wide
Official recall notice from HC-DEVICES
Recall details on Nibble Recalls: https://trynibble.app/recalls/7f0f9eff-b006-4cf5-9820-50ff11465d87