Rtis Devices (2016-12-14)

Artis Devices Recall Summary Artis Devices medical equipment has been recalled across Canada due to a safety or performance issue with the devices. This is classified as a Class I recall, which indicates a serious problem. The recall affects devices that were distributed throughout Canada.

Reason

Medical devices

Classification

Class I

Category

drug recall

Country

Canada

Agency

HC-DEVICES

Recall date

2017-01-06

Status

Closed

Distribution

Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/9b995d91-e621-45aa-b2cc-a0740643aef1