Vitros 5600 Integrated System (2016-02-17)

Recall Summary The VITROS 5600 Integrated System, a medical laboratory device, has been recalled in Canada due to a safety or performance issue. This Class I recall affects the device across Canada and applies to the healthcare facilities and laboratories that use this equipment.

Reason
Medical devices
Classification
Class I
Category
drug recall
Country
Canada
Agency
HC-DEVICES
Recall date
2016-03-04
Status
Closed
Distribution
Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/52307d10-e9c8-48f6-90fa-9bb0922ab370