Ortic Arch Cannulae (2016-07-13)
Aortic Arch Cannulae Recall Summary Aortic arch cannulae (tubes used during heart surgery to connect patients to bypass machines) are being recalled across Canada due to a device defect. The recall is classified as Class I, meaning there is a serious risk of adverse health consequences. 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
- 2016-08-16
- Status
- Closed
- Distribution
- Canada-wide
Official recall notice from HC-DEVICES
Recall details on Nibble Recalls: https://trynibble.app/recalls/6c6f50ed-9ead-4f38-a217-57d216e16354