BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    MAXI MOVE

    MDR report key: 1942032 · Received November 8, 2010

    Report

    Report Number
    9681684-2010-00047
    Event Type
    Malfunction
    Date Received
    November 8, 2010
    Date of Event
    October 8, 2010
    Report Date
    October 11, 2010
    Manufacturer
    BHM MEDICAL, INC.
    Product Code
    FSA
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    MS, US
    Reporter Occupation
    NOT APPLICABLE

    Narratives

    Additional Manufacturer Narrative · 1

    FURTHER INFO WILL BE PROVIDED UPON MFR'S INVESTIGATION.

    Description of Event or Problem · 1

    THE NURSES WERE LIFTING A FEMALE PT WITHOUT LEGS OUT OF THE BED. WHILE THE LIFT WAS UP AND THE PT SUSPENDED IN AIR, THE LIFT MADE A NOISE AND THE JIB SLID STRAIGHT DOWN WITH THE PT STILL IN THE SLING, CAUSING THE PT TO FALL ONTO THE BED. NO INJURIES WERE SUSTAINED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 MAXI MOVE LIFT, PATIENT, NON-AC POWERED FSA BHM MEDICAL, INC. KMCSUN

    Patients

    Seq Age Sex Outcome Treatment
    1 Other