Cobas P612 And P512 Pre-analytical Systems (2017-05-31)

Cobas P612 and P512 Pre-Analytical Systems Recall Roche Diagnostics is recalling Cobas P612 and P512 Pre-Analytical Systems across Canada because of a potential defect that could affect how patient blood samples are processed. These are laboratory instruments used in hospitals and diagnostic facilities to prepare blood samples for testing. This is classified as a serious safety issue affecting all units distributed in Canada.

Reason

Medical devices

Classification

Class I

Category

drug recall

Country

Canada

Agency

HC-DEVICES

Recall date

2017-06-21

Status

Closed

Distribution

Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/976929d0-59fa-4704-829e-5c3c80d92691