Cobas H 232 Instruments (2016-04-26)

COBAS H 232 Instruments Recall Roche Diagnostics is recalling COBAS H 232 laboratory instruments distributed across Canada due to a software issue that could cause incorrect test results. The affected devices are used in hospitals and laboratories to analyze blood samples. This is a Class I recall, indicating a serious potential for harm.

Reason

Medical devices

Classification

Class I

Category

drug recall

Country

Canada

Agency

HC-DEVICES

Recall date

2016-05-16

Status

Closed

Distribution

Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/61e2162b-0d65-4c5e-b2b4-185bf519c977