Aesculap Ag Haemostatic Forceps
Recall Summary Aesculap AG Haemostatic Forceps are being recalled across Canada due to a performance issue with the product. This recall affects all haemostatic forceps distributed by Aesculap AG in Canada. The recall is classified as Class I, which indicates a serious safety concern.
- Product
- Aesculap AG Haemostatic Forceps
- Reason
- Performance
- Classification
- Class I
- Category
- drug recall
- Country
- Canada
- Agency
- HC-DEVICES
- Recall date
- 2025-02-06
- Status
- Ongoing
- Distribution
- Canada-wide
Official recall notice from HC-DEVICES
Recall details on Nibble Recalls: https://trynibble.app/recalls/033dbb54-d3c2-4ed2-9e6e-22cab51cf87a