Iom Artis, Zee, Q, Q.zen Devices (2017-06-06)

Axiom Artis, Zee, Q, and Q.Zen Devices Recall Axiom Artis, Zee, Q, and Q.Zen medical devices are being recalled in Canada due to a safety issue with the devices. This Class I recall affects devices that were distributed across Canada. The devices are classified as drugs for regulatory purposes.

Reason

Medical devices

Classification

Class I

Category

drug recall

Country

Canada

Agency

HC-DEVICES

Recall date

2017-07-06

Status

Closed

Distribution

Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/3c77e325-a801-4dc9-a1da-944f6f7fbb89