Llura Xper Systems (2017-03-17)

Allura XPER Systems Recall Summary Allura XPER Systems medical devices are being recalled across Canada due to a safety issue. The recall is classified as Class I, which indicates a serious problem with the device. This recall affects all Canadian users of these medical devices.

Reason

Medical devices

Classification

Class I

Category

drug recall

Country

Canada

Agency

HC-DEVICES

Recall date

2017-04-13

Status

Closed

Distribution

Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/c65fa45f-6e55-4e14-a435-f413fa33a081