BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    LIKORALL OVERHEAD LIFT

    MDR report key: 24811018 · Received April 7, 2026

    Report

    Report Number
    8030916-2026-00038
    Event Type
    Malfunction
    Date Received
    April 7, 2026
    Date of Event
    December 19, 2025
    Report Date
    April 7, 2026
    Manufacturer
    BAXTER HEALTHCARE CORPORATION
    Product Code
    FSA
    UDI-DI
    00887761981911
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    SW
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 0

    THE SERVICE TECHNICIAN INSPECTED THE LIFT AND FOUND THAT IT WAS SHAFT BREAKAGE. A FUNCTIONAL TEST OF THE SINGLE FAULT SAFETY (SFS) SAFETY DRUM WAS PERFORMED. THE RESULT FROM THE TEST WAS THAT THE SFS SAFETY DRUM WAS FUNCTIONING AS DESIGNED. THIS MOTOR SHAFT BREAKAGE IS DETERMINED TO BE CAUSED BY A MECHANICAL MALFUNCTION. THE TECHNICIAN REPLACED THE LIFT WITH A NEW ONE TO RESOLVE THE REPORTED EVENT. BASED ON THIS INFORMATION, NO FURTHER ACTION IS REQUIRED. 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 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.

    Additional Manufacturer Narrative · 0

    NO FURTHER INFORMATION IS AVAILABLE ON THE REPAIR OF THE DEVICE AT THIS TIME. THE INVESTIGATION IS ONGOING, HOWEVER IF ANY ADDITIONAL RELEVANT INFORMATION IS IDENTIFIED FOLLOWING THE COMPLETION OF THE INVESTIGATION, THE ADDITIONAL RELEVANT INFORMATION IS IDENTIFIED FOLLOWING COMPLETION OF THE INVESTIGATION, THE ADDITIONAL RELEVANT INFORMATION WILL BE SUBMITTED IN A SUPPLEMENTAL REPORT.

    Description of Event or Problem · 0

    BAXTER RECEIVED A REPORT THAT LIKORALL 200 HAD A CEILING STRAP DETACHMENT, IT SUDDENLY DROPPED. 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
    868954 LIKORALL OVERHEAD LIFT LIFT, PATIENT, NON-AC-POWERED FSA BAXTER HEALTHCARE CORPORATION 3121001 00887761981911

    Patients

    Seq Age Sex Outcome Treatment
    1 NA Unknown