Llura Xper Fd10/10-main Unit

Recall Summary Allura XPER FD10/10-Main Unit devices are being recalled across Canada due to a defect that could cause them to malfunction. The affected devices may fail to operate properly, which could impact their intended use. This recall applies to all Allura XPER FD10/10-Main Unit devices distributed in Canada.

Classification

Class I

Category

drug recall

Country

Canada

Agency

HC-DEVICES

Recall date

2016-09-23

Status

Closed

Distribution

Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/0b476b6e-2f05-4de1-a93f-406da9c29dd4