Rtis Zee Multi-purpose, Artis Q (2019-04-22)

Artis Zee Multi-Purpose and Artis Q Recall Artis Zee Multi-Purpose and Artis Q medical devices are being recalled across Canada. The recall is classified as Class I, which is the most serious type. The specific reason for the recall relates to issues with these medical devices, though details about the particular defect are not provided in this notice.

Reason
Medical devices
Classification
Class I
Category
drug recall
Country
Canada
Agency
HC-DEVICES
Recall date
2019-05-24
Status
Ongoing
Distribution
Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/4e06e534-a3a6-420c-a3b6-08955895c092