BEUDAMED
    FDA Adverse Event Injury Summary report: N

    MAXI MOVE

    MDR report key: 3251915 · Received July 22, 2013

    Report

    Report Number
    1419652-2013-00201
    Event Type
    Injury
    Date Received
    July 22, 2013
    Date of Event
    July 8, 2013
    Report Date
    July 8, 2013
    Manufacturer
    ARJO HOSP EQUIPMENT AB
    Product Code
    FSA
    Adverse Event
    Yes
    Product Problem
    Yes
    Report Source
    Distributor report
    Reporter Location
    FL, US
    Reporter Occupation
    OTHER

    Narratives

    Description of Event or Problem · 1

    PT WAS BEING LIFTED WITH DISPOSABLE SLING THAT HAD BEEN LAUNDERED. AS SHE WAS BEING RAISED, RIGHT LEG CLIP DETACHED FROM LIFT AND PT FELL ON THE FLOOR. (B)(4).

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    340244 MAXI MOVE FSA ARJO HOSP EQUIPMENT AB MAXI MOVE II

    Patients

    Seq Age Sex Outcome Treatment
    1 80 YR