Bl800 Flex System - Instrument Configurations (2020-02-24)

ABL800 FLEX System Recall Summary The ABL800 FLEX blood gas analyzer system is being recalled across Canada due to a medical device issue. This recall affects hospital and laboratory settings that use this diagnostic instrument. The recall is classified as Class I, indicating a serious potential health risk.

Reason
Medical devices
Classification
Class I
Category
drug recall
Country
Canada
Agency
HC-DEVICES
Recall date
2020-03-06
Status
Ongoing
Distribution
Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/858ec10d-3107-47b7-b43d-24b138986128