BEUDAMED
    FDA Adverse Event Other Summary report: N

    GIRAFFE OMNIBED

    MDR report key: 546629 · Received September 27, 2004

    Report

    Report Number
    1121732-2004-00012
    Event Type
    Other
    Date Received
    September 27, 2004
    Report Date
    September 27, 2004
    Manufacturer
    OHMEDA MEDICAL
    Product Code
    FMZ
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    WI, US
    Reporter Occupation
    OTHER

    Narratives

    Description of Event or Problem · 1

    IT WAS REPORTED THAT THE ELEVATING BASE OF A GIRAFFE OMNIBED INADVERTENTLY LOWERED WITH A PT IN THE UNIT AFTER A POWER FAILURE. THE ELEVATING BASE LOWERED TO THE BOTTOM STOP POSITION. NO INJURY WAS REPORTED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 GIRAFFE OMNIBED INFANT THERMOREGULATION FMZ OHMEDA MEDICAL * *

    Patients

    Seq Age Sex Outcome Treatment
    1 UNKNOWN Other