BEUDAMED
    FDA Adverse Event Death Summary report: N

    500 LB SMART LIFT

    MDR report key: 25173528 · Received May 14, 2026

    Report

    Report Number
    2183887-2026-00007
    Event Type
    Death
    Date Received
    May 14, 2026
    Date of Event
    May 3, 2026
    Report Date
    May 14, 2026
    Manufacturer
    EZ WAY INC
    Product Code
    FSA
    UDI-DI
    00848914000040
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    MN, US
    Reporter Occupation
    NURSE
    Health Professional
    Yes

    Narratives

    Additional Manufacturer Narrative · 0

    THE FAMILY HAD A CAMERA TO RECORD INTERACTIONS WITH THE RESIDENT AND RECORDED THIS INCIDENT.

    Description of Event or Problem · 0

    CNA WAS ON EACH SIDE OF BED, HOOKING UP STRAPS TO THE LIFT. THE CNA ON THE SIDE OF THE BED WITH THE MACHINE HOOKED UP A LOOP TO THE LIFT AND MOVED TO THE OTHER SIDE OF THE BED. WHILE MOVING TO THE OTHER SIDE, THE CNA WAS PICKING THINGS UP AND MOVING THINGS AND ONE OF THE LEG LOOPS DID NOT GET HOOKED UP TO THE MACHINE. WHEN THE RESIDENT WAS LIFTED OFF THE BED, SHE SLID OUT OF THE SLING. THE RESIDENT DIED THE NEXT DAY. (B)(6) SAID THE LIFT WAS NOT AT FAULT AND THIS WAS USER ERROR.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    49464 500 LB SMART LIFT LIFT FSA EZ WAY INC L500PN-03 00848914000040

    Patients

    Seq Age Sex Outcome Treatment
    1 91 YR Female Death