Zurion 7 M20 (2020-03-03)

Recall Summary Azurion 7 M20 devices have been recalled across Canada due to a medical device issue. This recall is classified as Class I, meaning there is a serious potential health risk. The recall affects all Azurion 7 M20 devices distributed in Canada.

Reason

Medical devices

Classification

Class I

Category

drug recall

Country

Canada

Agency

HC-DEVICES

Recall date

2020-04-15

Status

Ongoing

Distribution

Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/ce6dc09c-2560-4858-b602-9f9a7dacd3cb