Multidiagnost Eleva - Image Intensifier And Flat Detector, Allura Xper (fd10, Fd20, Fd20/10, Fd20/15, Fd20/20) (2019-02-24)

Recall Summary Philips is recalling certain MultiDiagnost Eleva image intensifier and flat detector systems used in ALLURA XPER equipment across Canada due to a medical device issue. These are X-ray imaging systems used in hospitals and medical facilities. This is classified as a Class I recall, which indicates a serious potential health risk.

Reason

Medical devices

Classification

Class I

Category

drug recall

Country

Canada

Agency

HC-DEVICES

Recall date

2019-03-08

Status

Ongoing

Distribution

Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/9a317efd-6cec-4211-a346-64eba3dada67