Balloon Guide Catheter (2018-11-13)

Balloon Guide Catheter Recall Summary A Balloon Guide Catheter medical device is being recalled across Canada. The device is being recalled due to safety or performance concerns that classify it as a Class I recall, the most serious type. The recall affects users of this catheter throughout Canada.

Reason

Medical devices

Classification

Class I

Category

drug recall

Country

Canada

Agency

HC-DEVICES

Recall date

2019-01-09

Status

Ongoing

Distribution

Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/3e0deed8-812d-4e2e-adf1-291734fd00fb