Rtis Q (2019-07-31)

Artis Q Recall Summary Artis Q medical devices are being recalled across Canada due to a safety issue that requires Class I classification (the most serious level). The recall affects all Artis Q devices that were distributed in Canada.

Reason
Medical devices
Classification
Class I
Category
drug recall
Country
Canada
Agency
HC-DEVICES
Recall date
2019-08-23
Status
Ongoing
Distribution
Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/2e3fc037-ea73-4923-9f18-756d121f8821