Stryker Instruments Break-away Femoral Nozzle
Recall Summary Stryker Instruments is recalling Break-away Femoral Nozzles across Canada because they may not perform as intended. This recall affects medical devices used in surgical procedures and has been classified as a Class I recall, the most serious category.
- Product
- Stryker Instruments Break-away Femoral Nozzle
- Reason
- Performance
- Classification
- Class I
- Category
- drug recall
- Country
- Canada
- Agency
- HC-DEVICES
- Recall date
- 2023-08-16
- Status
- Ongoing
- Distribution
- Canada-wide
Official recall notice from HC-DEVICES
Recall details on Nibble Recalls: https://trynibble.app/recalls/71611f98-2335-48cf-b44e-c9aa392fab96