BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    ALLIA

    MDR report key: 24144379 · Received January 22, 2026

    Report

    Report Number
    24144379
    Event Type
    Malfunction
    Date Received
    January 22, 2026
    Date of Event
    January 5, 2026
    Report Date
    January 6, 2026
    Manufacturer
    GE HEALTHCARE TECHNOLOGIES, INC.
    Product Code
    OWB
    Product Problem
    Yes
    Report Source
    User Facility report
    Reporter Location
    AZ
    Reporter Occupation
    OTHER HEALTH CARE PROFESSIONAL
    Health Professional
    Yes

    Narratives

    Description of Event or Problem · 0

    WHILE TRANSFERRING PATIENT FROM GURNEY TO THE GE X-RAY TABLE, THE BRAKES FAILED ON THE GE XRAY TABLE AND MOVED WHEN STAFF TRANSFERRING PATIENT. THE BED WAS STABILIZED BY 3 STAFF MEMBERS ON EITHER SIDE OF THE TABLE. MESSAGE ON SCREEN: "TABLE TOP BRAKES FAILURE". PATIENT WAS SAFE AND STAFF ASSISTED CORRECTLY. STAFF RE-STARTED X-RAY TWICE HOWEVER ERROR MESSAGE REMAINED ON SCREEN. BRAKE WORKED FINE AFTER INCIDENT. MANAGER WAS NOTIFIED, BIOMED TICKET WAS PLACED, AS WELL AS GE REP NOTIFIED. GE RESPONDED THEY ARE AWARE OF THE ISSUE AT A NATIONAL LEVEL. GE WILL ISSUE A SOFTWARE CORRECTION. GE DOES NOT HAVE A RELEASE DATE FOR THEIR SOFTWARE CORRECTION.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    204028 ALLIA INTERVENTIONAL FLUOROSCOPIC X-RAY SYSTEM OWB GE HEALTHCARE TECHNOLOGIES, INC.

    Patients

    Seq Age Sex Outcome Treatment
    1 68 YR Male