Bl800 Flex System - Instrument Configurations (2017-10-02)
ABL800 FLEX SYSTEM Recall Summary The ABL800 FLEX System instruments are being recalled across Canada due to a medical device issue. This is a Class I recall, which is the most serious classification. The affected devices were distributed nationwide in Canada.
- Reason
- Medical devices
- Classification
- Class I
- Category
- drug recall
- Country
- Canada
- Agency
- HC-DEVICES
- Recall date
- 2017-10-27
- Status
- Closed
- Distribution
- Canada-wide
Official recall notice from HC-DEVICES
Recall details on Nibble Recalls: https://trynibble.app/recalls/ae756f9c-fa93-460a-98fe-fe023eb9a9ab