Unicel Dxc 600i Clinical Analyzer (2017-03-13)

Unicel DxC 600i Clinical Analyzer Recall Unicel DxC 600i Clinical Analyzers, used in laboratories to process patient blood and body fluid samples, are being recalled across Canada. The devices have been identified as posing a medical device safety concern. This recall affects laboratory facilities and healthcare institutions that use this analyzer model.

Reason

Medical devices

Classification

Class I

Category

drug recall

Country

Canada

Agency

HC-DEVICES

Recall date

2017-03-31

Status

Closed

Distribution

Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/0ebecc52-0b03-424b-99ac-7da59af8a336