Cobas® C 303 Analytical Unit

Cobas c 303 Analytical Unit Recall Roche Diagnostics GmbH is recalling the Cobas c 303 analytical unit in Canada due to a device performance issue. This recall affects laboratory equipment used for clinical analysis. The recall is classified as Class II, meaning the device could cause serious health consequences or death, though this is unlikely.

Product

cobas® c 303 analytical unit

Reason

Device performance issue

Classification

Class II

Category

medical device recall

Country

Canada

Agency

HC-DEVICES

Recall date

2026-10-15

Status

Ongoing

Distribution

Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/6f43969c-3c63-4885-ae57-1f0745c6c138