BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    LIKORALL 200

    MDR report key: 23405495 · Received October 28, 2025

    Report

    Report Number
    8030916-2025-00125
    Event Type
    Malfunction
    Date Received
    October 28, 2025
    Date of Event
    October 2, 2025
    Report Date
    February 19, 2026
    Manufacturer
    BAXTER HEALTHCARE CORPORATION
    Product Code
    FSA
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    OH, US
    Reporter Occupation
    OTHER
    Health Professional
    N

    Narratives

    Additional Manufacturer Narrative · 0

    ADDITIONAL INFORMATION HAS BEEN REQUESTED REGARDING THE REPORTED MALFUNCTION. A FINAL REPORT WILL BE SUBMITTED UPON COMPLETION OF THE INVESTIGATION.

    Additional Manufacturer Narrative · 0

    UPON INSPECTION, THE BAXTER TECHNICIAN FOUND THE BATTERY NEEDED TO BE REPLACED. 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. A REPLACEMENT BATTERY WAS SENT TO THE CUSTOMER. BASED ON THIS INFORMATION, NO FURTHER ACTION IS REQUIRED. ALTHOUGH THERE WAS NO REPORTED INJURY WITH THIS EVENT, IF THE REPORT OF AN EMERGENCY FUNCTION OPERATIVE WERE TO RECUR, IT COULD POTENTIALLY CAUSE SERIOUS INJURY OR DEATH. THEREFORE, BAXTER IS REPORTING THIS EVENT.

    Description of Event or Problem · 0

    A OTHER HEALTH CARE PROFESSIONAL CONTACTED TECHNICAL SERVICE TO REPORT THAT THE LIKORALL 200 UNIT WILL NOT GO DOWN (APPEARS IN FULL UP POSITION) AND EMERGENCY/RELEASE STOP DOESN'T OPERATE. THE PROCESS STEP DURING WHICH THIS OCCURRED WAS UNKNOWN. 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
    50175 LIKORALL 200 LIFT PATIENT NON AC POWERED FSA BAXTER HEALTHCARE CORPORATION 3121001 NA

    Patients

    Seq Age Sex Outcome Treatment
    1 NA Unknown N/A.