Ortic Arch Cannulae (2017-06-23)

Aortic Arch Cannulae Recall Summary Aortic arch cannulae (tubes used during heart surgery) are being recalled across Canada due to a device defect. The recall is classified as Class I, meaning there is a serious potential health risk. This recall affects medical devices that were distributed throughout Canada.

Reason

Medical devices

Classification

Class I

Category

drug recall

Country

Canada

Agency

HC-DEVICES

Recall date

2017-06-30

Status

Closed

Distribution

Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/44563756-1832-4072-ad89-9cea37108431