Luminos Drf Max, Uroskop Omnia Max, Multitom Rax

Recall Summary Three X-ray imaging systems (LUMINOS DRF MAX, UROSKOP OMNIA MAX, and MULTITOM RAX) are being recalled across Canada due to a software defect. This is a Class I recall, meaning there is a serious potential health risk. The recall affects medical facilities that use these devices.

Product

LUMINOS DRF MAX, UROSKOP OMNIA MAX, MULTITOM RAX

Reason

Software defect

Classification

Class I

Category

drug recall

Country

Canada

Agency

HC-DEVICES

Recall date

2022-04-11

Status

Ongoing

Distribution

Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/fa9981bf-1b91-4fc7-ac45-f0cef9f32fd3