Rtis Q And Artis Q.zen (2018-07-30)

Artis Q and Artis Q.Zen Recall Summary Artis Q and Artis Q.Zen medical devices are being recalled across Canada due to a safety issue classified as Class I, which is the most serious type of recall. The specific reason for the recall relates to the devices' function or safety performance. This recall affects all Canadian consumers and healthcare facilities that have these devices.

Reason
Medical devices
Classification
Class I
Category
drug recall
Country
Canada
Agency
HC-DEVICES
Recall date
2018-08-17
Status
Ongoing
Distribution
Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/551626f9-9ae1-441a-93c6-dfba31e17e9b