Vitek 2 Systems And Compact Systems (2017-11-21)
Vitek 2 Systems and Compact Systems Recall Vitek 2 Systems and Compact Systems medical devices are being recalled across Canada. The FDA classified this as a Class I recall, indicating a serious issue with the device. The specific reason for the recall relates to the medical device classification, though details on the particular safety concern are not provided in this notice.
- Reason
- Medical devices
- Classification
- Class I
- Category
- drug recall
- Country
- Canada
- Agency
- HC-DEVICES
- Recall date
- 2017-12-08
- Status
- Closed
- Distribution
- Canada-wide
Official recall notice from HC-DEVICES
Recall details on Nibble Recalls: https://trynibble.app/recalls/dd8dd5b1-2e70-449a-800e-c93940118421