Ia-360 Immunoassay Analyzer System (2018-12-29)

Recall Summary The AIA-360 Immunoassay Analyzer System is being recalled in Canada due to a defect classified as Class I, which is the most serious type. This device is used in medical laboratories to run diagnostic tests. The recall affects all units distributed across Canada.

Reason

Medical devices

Classification

Class I

Category

drug recall

Country

Canada

Agency

HC-DEVICES

Recall date

2019-01-23

Status

Ongoing

Distribution

Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/288fa670-a9fa-43f8-b3e5-9f73e5f07492