Cobas H 232 Instruments (2019-10-22)

Cobas H 232 Instruments Recall Summary Roche Diagnostics is recalling Cobas H 232 hematology analyzers in Canada due to a software issue that could cause inaccurate blood test results. The recall affects laboratory facilities across Canada that use this instrument for patient blood testing. This is classified as a Class I recall, indicating a serious potential health risk.

Reason

Medical devices

Classification

Class I

Category

drug recall

Country

Canada

Agency

HC-DEVICES

Recall date

2020-01-06

Status

Ongoing

Distribution

Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/9de4468f-7866-4913-bf92-02f925e46021