BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    MEDILIFTER 4

    MDR report key: 1171337 · Received September 17, 2008

    Report

    Report Number
    9681684-2008-00025
    Event Type
    Malfunction
    Date Received
    September 17, 2008
    Date of Event
    July 31, 2008
    Report Date
    September 16, 2008
    Manufacturer
    BHM MEDICAL, INC.
    Product Code
    FNG
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    CA
    Reporter Occupation
    NOT APPLICABLE

    Narratives

    Description of Event or Problem · 1

    THE FACILITY REPORTS THEY WERE TRANSFERRING THE RESIDENT FROM THE BED TO THE CHAIR, BACKING INTO THE DOOR OPENING TO THE WASHROOM. WHEN TURNING THE LIFT TO DIRECT IT TOWARDS THE WHEELCHAIR, IT TIPPED OVER. THE STAFF EASED THE LIFT AND RESIDENT TO THE GROUND. NO INJURIES WERE REPORTED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 MEDILIFTER 4 PATIENT LIFT FNG BHM MEDICAL, INC. 7050-1000

    Patients

    Seq Age Sex Outcome Treatment
    1