BEUDAMED
    FDA Adverse Event Death Summary report: N

    500 LB PREMIER LIFT WITHOUT SCALE

    MDR report key: 25203772 · Received May 18, 2026

    Report

    Report Number
    2183887-2026-00008
    Event Type
    Death
    Date Received
    May 18, 2026
    Date of Event
    May 8, 2026
    Report Date
    May 18, 2026
    Manufacturer
    EZ WAY INC
    Product Code
    FSA
    UDI-DI
    00848914000040
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    NE, US
    Reporter Occupation
    NURSE
    Health Professional
    Yes

    Narratives

    Description of Event or Problem · 0

    STAFF WAS GOING FROM BED TO WHEELCHAIR. THEY HAD A SIDE ENTRANCE AND THE LIFT TIPPED DURING PROCESS. THE RESIDENT FELL ON FLOOR STILL IN THE SLING. THEY HAD TO UNHOOK THE SLING TO GET RESIDENT OUT AND BACK UP. THE RESIDENT BROKE HER HIP.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    240286 500 LB PREMIER LIFT WITHOUT SCALE LIFT FSA EZ WAY INC 798 00848914000040

    Patients

    Seq Age Sex Outcome Treatment
    1 81 YR Female Death