Cobas P 671 (2020-04-29)

Cobas p 671 Recall Summary The Cobas p 671 medical device has been recalled across Canada due to a safety or performance issue. This is a Class I recall, which is the most serious classification. The specific reason for the recall relates to the device's function as a medical device used in laboratory or clinical settings.

Reason
Medical devices
Classification
Class I
Category
drug recall
Country
Canada
Agency
HC-DEVICES
Recall date
2020-06-05
Status
Ongoing
Distribution
Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/715fd353-7b38-4814-8b42-b506082539d3