Rtis Zee Biplane, Artis Q And Artis Q.zen (2018-10-24)

Recall Summary Artis zee biplane, Artis Q, and Artis Q.zen medical devices are being recalled across Canada due to a defect classified as a Class I recall, which indicates a serious safety issue. These devices were distributed throughout Canada and are used in medical procedures. Affected users should contact their healthcare provider or the manufacturer for specific instructions regarding their device.

Reason

Medical devices

Classification

Class I

Category

drug recall

Country

Canada

Agency

HC-DEVICES

Recall date

2018-11-02

Status

Ongoing

Distribution

Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/327b3692-59e5-494f-a710-94b8d3204f0f