Bl800 Flex Analyzer (2020-05-07)

ABL800 FLEX Analyzer Recall Summary The ABL800 FLEX Analyzer, a medical device used for blood testing, is being recalled across Canada due to a safety issue. This recall affects healthcare facilities and laboratories that use this analyzer. The recall is classified as Class I, which indicates a serious potential health risk.

Reason

Medical devices

Classification

Class I

Category

drug recall

Country

Canada

Agency

HC-DEVICES

Recall date

2020-11-20

Status

Ongoing

Distribution

Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/eba92d95-a316-4ef1-8282-bdcafca0f949