Cobas 8000 Core Unit (2017-07-20)

Recall Summary Roche Diagnostics' COBAS 8000 CORE UNIT laboratory analyzer has been recalled across Canada due to a medical device issue. The device is used in clinical laboratories to process patient samples for diagnostic testing.

Reason

Medical devices

Classification

Class I

Category

drug recall

Country

Canada

Agency

HC-DEVICES

Recall date

2017-11-10

Status

Closed

Distribution

Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/7511cd81-46c6-4a8a-9fbc-3e9c1f3ab712