Rtis Systems (2017-02-22)

Artis Systems Recall Summary Artis Systems medical devices have been recalled across Canada due to safety concerns. The recall is classified as Class I, which is the most serious type. The specific details about which devices are affected and the exact nature of the safety issue are not provided in this summary information.

Reason

Medical devices

Classification

Class I

Category

drug recall

Country

Canada

Agency

HC-DEVICES

Recall date

2017-03-24

Status

Closed

Distribution

Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/d9b2c9d3-293b-4197-9d00-4659a81dd9e5