Bl800 Flex Analyzer (2018-06-25)
ABL800 Flex Analyzer Recall Summary The ABL800 Flex Analyzer, a medical device used for blood testing, has been recalled across Canada due to a device safety issue. This recall affects units distributed throughout the country. The recall is classified as Class I, which is the most serious classification level.
- Reason
- Medical devices
- Classification
- Class I
- Category
- drug recall
- Country
- Canada
- Agency
- HC-DEVICES
- Recall date
- 2018-07-05
- Status
- Ongoing
- Distribution
- Canada-wide
Official recall notice from HC-DEVICES
Recall details on Nibble Recalls: https://trynibble.app/recalls/a3d3f5bc-3b23-4178-b17f-baab686a3c75