BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    LIKORALL OVERHEAD LIFT

    MDR report key: 24307678 · Received February 10, 2026

    Report

    Report Number
    8030916-2026-00012
    Event Type
    Malfunction
    Date Received
    February 10, 2026
    Date of Event
    January 15, 2026
    Report Date
    March 17, 2026
    Manufacturer
    BAXTER HEALTHCARE CORPORATION
    Product Code
    FSA
    UDI-DI
    00887761981911
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    FI
    Reporter Occupation
    OTHER
    Health Professional
    N

    Narratives

    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 COMPLETION OF THE INVESTIGATION, THE ADDITIONAL RELEVANT INFORMATION WILL BE SUBMITTED IN A SUPPLEMENTAL REPORT.

    Additional Manufacturer Narrative · 0

    THE BAXTER TECHNICIAN FOUND THE MOTOR SHAFT BROKEN. 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. THE ISSUE WAS RESOLVED BY PROVIDING THE CUSTOMER WITH A NEW LIFT.

    Description of Event or Problem · 0

    ON 15-JAN-2026, A DISTRIBUTOR CONTACTED TECHNICAL SERVICE TO REPORT THAT LIKORALL 200 (PRODUCT CODE 3121001, SERIAL NUMBER (B)(6)), THE AXLE BETWEEN THE MOTOR AND SAFETY DRUM BROKE AND FOR THAT REASON PATIENT DROPPED APPROX 25-30CM. 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
    364083 LIKORALL OVERHEAD LIFT LIFT, PATIENT, NON-AC-POWERED FSA BAXTER HEALTHCARE CORPORATION 3121001 00887761981911

    Patients

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