BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    LIKORALL 200

    MDR report key: 22182462 · Received June 11, 2025

    Report

    Report Number
    8030916-2025-00079
    Event Type
    Malfunction
    Date Received
    June 11, 2025
    Date of Event
    May 22, 2025
    Report Date
    June 11, 2025
    Manufacturer
    BAXTER HEALTHCARE CORPORATION
    Product Code
    FSA
    UDI-DI
    00887761981911
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    FR
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 0

    THE BAXTER TECHNICIAN REPLACED THE EMERGENCY STOP BUTTON. LIKORALL OVERHEAD LIFT IS A STATIONARY LIFT MOUNTED IN A RAIL SYSTEM. THE RAIL SYSTEM CAN BE BUILT STRAIGHT, WITH OR WITHOUT CURVES, AS A TRAVERSE SYSTEM AND ALSO AS A ROOM-TO-ROOM SYSTEM. LIKORALL OVERHEAD LIFT IS INTENDED FOR USE IN LIFTING AND TRANSFERRING PATIENTS, FOR EXAMPLE, FROM BED TO A WHEELCHAIR, TO OR FROM THE FLOOR, FOR VISITS TO THE TOILET, FOR GAIT, STANDING AND BALANCE TRAINING, WHEN WEIGHING THE PATIENT AND WHEN LIFTING THE PATIENT WITH A STRETCHER. ALTHOUGH THERE WAS NO ADVERSE EVENT REPORTED, A REPORT OF A EMERGENCY STOP FUNCTION NOT WORKING IN AN OPERATIVE LIFT IS LIKELY TO CAUSE OR CONTRIBUTE TO A DEATH OR SERIOUS INJURY.

    Description of Event or Problem · 0

    THE CUSTOMER REQUESTED REPAIR FOR A FAULTY LIKORALL 200 LIFT. UPON INSPECTION, THE BAXTER TECHNICIAN FOUND THE EMERGENCY STOP BUTTON WAS BROKEN. THERE WAS NO PATIENT/USER INJURY, MEDICAL INTERVENTION, SYMPTOM, OR ADVERSE EVENT REPORTED. THERE WERE NO OTHER DEVICES REPORTED TO BE INVOLVED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    86366 LIKORALL 200 LIFT PATIENT NON AC POWERED FSA BAXTER HEALTHCARE CORPORATION 3121001 00887761981911

    Patients

    Seq Age Sex Outcome Treatment
    1 NA Unknown