BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    MAXI MOVE

    MDR report key: 1220263 · Received October 31, 2008

    Report

    Report Number
    9611530-2008-00061
    Event Type
    Malfunction
    Date Received
    October 31, 2008
    Date of Event
    September 9, 2008
    Report Date
    October 30, 2008
    Manufacturer
    ARJO HOSPITAL EQUIPMENT AB
    Product Code
    FSA
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    UK
    Reporter Occupation
    NOT APPLICABLE

    Narratives

    Description of Event or Problem · 1

    THE FACILITY REPORTS THE PT WAS SEATED WITH THE SLING AROUND THEM. THE HOIST WAS LOWERED TO ATTACH TO THE SLING. THE JIB THEN DROPPED APPROXIMATELY TWO INCHES AND STRUCK THE CARER ON TOP OF THE HEAD. NO FURTHER INJURIES WERE SUSTAINED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 MAXI MOVE PT LIFTER FSA ARJO HOSPITAL EQUIPMENT AB KMBB4XXXXXXX

    Patients

    Seq Age Sex Outcome Treatment
    1