BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    LIKORALL OVERHEAD LIFT

    MDR report key: 24120565 · Received January 20, 2026

    Report

    Report Number
    8030916-2026-00007
    Event Type
    Malfunction
    Date Received
    January 20, 2026
    Date of Event
    December 23, 2025
    Report Date
    March 19, 2026
    Manufacturer
    BAXTER HEALTHCARE CORPORATION
    Product Code
    FSA
    UDI-DI
    00887761979468
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    SW
    Reporter Occupation
    OTHER
    Health Professional
    N

    Narratives

    Additional Manufacturer Narrative · 0

    THE INVESTIGATION IS ONGOING. ALL ADDITIONAL AND RELEVANT INFORMATION THAT IS IDENTIFIED FOLLOWING COMPLETION OF THE INVESTIGATION WILL BE SUBMITTED IN A FINAL REPORT.

    Additional Manufacturer Narrative · 0

    BAXTER HAS CONTACTED THE ACCOUNT THREE TIMES REQUESTING THE DEVICE TO BE RETURNED FOR INSPECTION. THE ACCOUNT WAS UNRESPONSIVE TO THE ATTEMPTS AND THE DEVICE DID NOT RETURN TO MANUFACTURE. THEREFORE, BAXTER IS COMPLETING THIS COMPLAINT DUE TO THE AMOUNT OF TIME. BASED ON THIS INFORMATION, NO FURTHER ACTION IS REQUIRED. LIKORALL OVERHEAD LIFT IS INTENDED FOR USE IN, HEALTH CARE, INTENSIVE CARE AND REHABILITATION. LIKORALL OVERHEAD LIFT IS DESIGNED FOR FIXED INSTALLATION AND FREE-STANDING LIFT SYSTEMS. ALL COMMON LIFTS AND TRANSFERS CAN BE PERFORMED USING LIKORALL OVERHEAD LIFT, FOR INSTANCE BETWEEN BED/WHEELCHAIR, TO/FROM FLOOR, TOILET VISITS, GAIT TRAINING, AND TOGETHER WITH STRETCHERS. LIKORALL R2R (ROOM TO ROOM) OVERHEAD LIFT ENABLES THE PATIENT TO BE MOVED BETWEEN TWO RAIL SYSTEMS IN SEPARATE ROOMS. LIKORALL OVERHEAD LIFT WITH THE ES DESIGNATION IS PREPARED FOR OPERATION WITH THE WIRELESS HANDCONTROL REMOTE (IR) AND IN ADDITION, A TRANSFER MOTOR CAN BE CONNECTED FOR MOTOR DRIVEN MOVEMENT ALONG THE RAIL. LIKORALL S, IRC OVERHEAD LIFT IS PREPARED FOR CONTINUOUS CHARGING THROUGH THE RAILSYSTEM. A SEARCH OF THE BAXTER MAINTENANCE RECORDS DID NOT SHOW BAXTER PERFORMED ANY PREVENTATIVE MAINTENANCE ON THIS DEVICE. IT IS UNKNOWN IF THE FACILITY PERFORMS PREVENTATIVE MAINTENANCE ON THEIR DEVICE.

    Description of Event or Problem · 0

    ON 23-DEC-2025, A OTHER HEALTH CARE PROFESSIONAL CONTACTED TECHNICAL SERVICE TO REPORT THAT LIKORALL 242 S R2R, WHITE (PRODUCT CODE 3122012, SERIAL NUMBER (B)(6)), LIFT WAS TRANSFERRING A PATIENT WHEN IT STOPPED WORKING AND LET GO OF THE PATIENT WHO WAS ABOVE THE WHEELCHAIR. THIS OCCURRED DURING PATIENT USE. THERE WAS NO PATIENT/USER INJURY, MEDICAL INTERVENTION, SYMPTOM, OR ADVERSE EVENT REPORTED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    175132 LIKORALL OVERHEAD LIFT LIFT, PATIENT, NON-AC-POWERED FSA BAXTER HEALTHCARE CORPORATION 3122012 N/A 00887761979468

    Patients

    Seq Age Sex Outcome Treatment
    1 NA Unknown