Bl800 Flex System

ABL800 Flex System Recall Summary The ABL800 Flex System, a blood gas analyzer used in hospitals and labs, is being recalled across Canada due to a software issue that could cause incorrect test results. The malfunction may prevent the device from properly detecting certain critical blood gas values, potentially affecting patient care decisions. This recall applies to all ABL800 Flex Systems distributed throughout Canada.

Classification

Class I

Category

drug recall

Country

Canada

Agency

HC-DEVICES

Recall date

2017-02-01

Status

Closed

Distribution

Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/7c4a293e-44c1-4416-8fe6-ff37b6854a13