Aesculap Inc. Surgical Instrument Sets

Recall Summary Aesculap Inc. is recalling Surgical Instrument Sets distributed across Canada because they are unauthorized medical devices. This Class I recall means the devices pose a serious health risk. The affected products were distributed nationwide in Canada.

Product
Aesculap Inc. Surgical Instrument Sets
Reason
Unauthorised device
Classification
Class I
Category
drug recall
Country
Canada
Agency
HC-DEVICES
Recall date
2025-12-17
Status
Ongoing
Distribution
Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/cd8b7a09-e81f-4b65-a85a-f5a8f4214f54