Zurion 7 M20 (2020-04-09)

Azurion 7 M20 Recall Summary The Azurion 7 M20 medical device is being recalled in Canada due to a safety issue. This device is used in medical facilities across the country. This is a Class I recall, which is the most serious classification.

Reason

Medical devices

Classification

Class I

Category

drug recall

Country

Canada

Agency

HC-DEVICES

Recall date

2020-05-01

Status

Ongoing

Distribution

Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/2a8d61db-f7a6-4219-bd5c-7a85cd70d271