Cobas E801 Analyzer (2019-03-17)

Cobas e801 Analyzer Recall Summary The cobas e801 analyzer, a medical laboratory device, is being recalled across Canada due to a safety or performance issue. This recall is classified as Class I, meaning there is a serious risk associated with the device. The recall affects cobas e801 analyzers that were distributed throughout Canada.

Reason

Medical devices

Classification

Class I

Category

drug recall

Country

Canada

Agency

HC-DEVICES

Recall date

2019-03-26

Status

Ongoing

Distribution

Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/38afbb34-5d86-4cf9-985f-aca02039094f