Coaguchek Xs Pro And Plus, Cobas H 232 Instruments (2017-12-18)

CoaguChek XS Pro and Plus, Cobas H 232 Instruments Recall CoaguChek XS Pro and Plus blood coagulation monitoring devices and Cobas H 232 instruments are being recalled across Canada. The devices may not accurately measure blood coagulation levels due to a manufacturing issue. This recall affects patients who use these instruments to monitor their blood clotting.

Reason

Medical devices

Classification

Class I

Category

drug recall

Country

Canada

Agency

HC-DEVICES

Recall date

2018-01-29

Status

Ongoing

Distribution

Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/2ceac09e-29ff-4ed8-9403-1564d654ba6c