Cobas Integra 400 Plus (2020-03-23)

Recall Summary The COBAS INTEGRA 400 Plus analyzer is being recalled across Canada due to a medical device issue classified as Class I, the most serious type of recall. This device is used in laboratory settings to process and analyze clinical samples. The recall affects all units distributed in Canada.

Reason
Medical devices
Classification
Class I
Category
drug recall
Country
Canada
Agency
HC-DEVICES
Recall date
2020-04-17
Status
Ongoing
Distribution
Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/2f67a51a-b3f0-4176-bf65-a3913471c6b5