Llura Xper Fd10/10 - Main Unit, Fd20/10 System-main Unit, Fd20/20, Fd10, Fd20 System - Main Unit, Fd20 Or Table (2017-12-28)

Recall Summary Allura Xper FD10/10, FD20/10, FD20/20, FD10, FD20 System main units and tables manufactured in 2017 are being recalled across Canada. The recall involves medical imaging equipment that may have a malfunction affecting device performance. This recall applies to healthcare facilities and medical centers that use these devices.

Reason
Medical devices
Classification
Class I
Category
drug recall
Country
Canada
Agency
HC-DEVICES
Recall date
2018-01-29
Status
Ongoing
Distribution
Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/ce008b61-abea-4836-b019-1fdcadcba3cb