Ysio Max, Luminos Drf Max, And Uroskop Omnia Max (2018-12-11)

Recall Summary Philips is recalling Ysio Max, Luminos dRF Max, and Uroskop Omnia Max X-ray imaging systems across Canada due to a potential safety issue with the devices. These systems are used in medical facilities for diagnostic imaging procedures. The recall is classified as Class I, which indicates a serious potential health risk.

Reason

Medical devices

Classification

Class I

Category

drug recall

Country

Canada

Agency

HC-DEVICES

Recall date

2019-01-09

Status

Ongoing

Distribution

Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/4c382787-0c29-45ee-9977-9fbd630f21e6