Cobas 6500 - Cobas U Cuvette (2017-09-14)

Recall Summary Roche Diagnostics is recalling Cobas 6500 and Cobas U Cuvettes distributed across Canada due to a defect in the medical device. The cuvettes are used in laboratory testing equipment to hold samples during analysis. This Class I recall indicates the defect could potentially cause serious harm or death.

Reason

Medical devices

Classification

Class I

Category

drug recall

Country

Canada

Agency

HC-DEVICES

Recall date

2018-02-22

Status

Ongoing

Distribution

Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/3fc6030d-7c13-49cd-91db-123d3e1cb802