Rtis Zee Multi-purpose And 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 indicates a serious issue with the devices. The specific reason for the recall relates to the devices' classification as medical devices, though additional details about the safety concern are not provided in this notice.

Reason

Medical devices

Classification

Class I

Category

drug recall

Country

Canada

Agency

HC-DEVICES

Recall date

2019-05-17

Status

Ongoing

Distribution

Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/39ddbcae-77a3-4b91-aead-c0155c6702f5