Abl800 Flex System
Recall Summary The ABL800 Flex System, a drug-related medical device, is being recalled in Canada due to a performance issue. The recall affects all units distributed across Canada. This is classified as a Class I recall, which is the most serious category.
- Product
- ABL800 Flex System
- Reason
- Performance
- Classification
- Class I
- Category
- drug recall
- Country
- Canada
- Agency
- HC-DEVICES
- Recall date
- 2022-05-24
- Status
- Ongoing
- Distribution
- Canada-wide
Official recall notice from HC-DEVICES
Recall details on Nibble Recalls: https://trynibble.app/recalls/fcdcf704-1901-447a-9c31-db4b06092bce