Vitek® 2 Systems
VITEK® 2 Systems Recall Summary VITEK® 2 Systems are being recalled in Canada due to a performance issue with the equipment. The recall is classified as Class I, meaning there is a potential serious adverse health consequence. These systems are distributed across Canada and are used in clinical laboratories for microbial identification and testing.
- Product
- VITEK® 2 Systems
- Reason
- Device performance issue
- Classification
- Class II
- Category
- medical device recall
- Country
- Canada
- Agency
- HC-DEVICES
- Recall date
- 2026-01-21
- Status
- Ongoing
- Distribution
- Canada-wide
Official recall notice from HC-DEVICES
Recall details on Nibble Recalls: https://trynibble.app/recalls/5e80a396-ab75-4948-8963-16c2f2b42ea9