Ia -360 And Aia 600 II Systems (2016-07-13)

Recall Summary AIA-360 and AIA 600 II Systems are medical devices that have been recalled across Canada due to safety or performance concerns. This recall affects all units of these systems distributed in Canada. The devices are classified as Class I, which indicates a serious issue.

Reason

Medical devices

Classification

Class I

Category

drug recall

Country

Canada

Agency

HC-DEVICES

Recall date

2016-08-05

Status

Closed

Distribution

Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/db188d58-9ec3-408a-b1a7-e09852a52b35