BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    LIKORALL OVERHEAD LIFT

    MDR report key: 24463436 · Received February 26, 2026

    Report

    Report Number
    8030916-2026-00022
    Event Type
    Malfunction
    Date Received
    February 26, 2026
    Date of Event
    February 3, 2026
    Report Date
    February 26, 2026
    Manufacturer
    BAXTER HEALTHCARE CORPORATION
    Product Code
    FSA
    UDI-DI
    00887761981911
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    OH, US
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 0

    UPON INSPECTION, THE BAXTER TECHNICIAN FOUND THE STRAP AND MOTOR NEEDED TO BE REPLACED. VIKING L AND XL MOBILE LIFTS ARE TWO VERSATILE LIFT MODELS INTENDED MAINLY FOR USE IN HEALTH CARE, INTENSIVE CARE AND REHABILITATION. VIKING L AND XL MOBILE LIFTS ARE INTENDED FOR HEAVIER PATIENTS. BOTH MODELS ARE EXCELLENT AIDS IN DAILY TRANSFERS OF ADULTS AND BARIATRICS, FOR INSTANCE, LIFTING TO AND FROM WHEEL CHAIR, BED, TOILET AND FLOOR. THE BAXTER TECHNICIAN REPLACED THE STRAP AND MOTOR TO RESOLVE. BASED ON THIS INFORMATION, NO FURTHER ACTION IS REQUIRED. ALTHOUGH THERE WAS NO REPORTED INJURY WITH THIS EVENT, IF THE REPORT OF AN STRAP FALL WERE TO RECUR, IT COULD POTENTIALLY CAUSE SERIOUS INJURY OR DEATH. THEREFORE BAXTER IS REPORTING THIS EVENT.

    Description of Event or Problem · 0

    OTHER HEALTH CARE PROFESSIONAL CONTACTED TECHNICAL SERVICE TO REPORT THAT LIKORALL 200 (PRODUCT CODE 3121001, SERIAL NUMBER (B)(6)), LIFT ALLOWED STRAP TO QUICKLY DESCEND CAUSING PATIENT TO HIT THE FLOOR. 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
    526650 LIKORALL OVERHEAD LIFT LIFT, PATIENT, NON-AC-POWERED FSA BAXTER HEALTHCARE CORPORATION 3121001 00887761981911

    Patients

    Seq Age Sex Outcome Treatment
    1 NA Unknown