BEUDAMED
    FDA Adverse Event Injury Summary report: N

    GIRAFFE INF WARMER

    MDR report key: 3467489 · Received November 8, 2013

    Report

    Report Number
    MW5032698
    Event Type
    Injury
    Date Received
    November 8, 2013
    Date of Event
    October 9, 2013
    Report Date
    November 7, 2013
    Manufacturer
    GE HEALTHCARE
    Product Code
    FMT
    Product Problem
    Yes
    Report Source
    Voluntary report
    Reporter Location
    CA, US
    Reporter Occupation
    NURSE

    Narratives

    Description of Event or Problem · 1

    A (B)(6) INFANT ADMITTED TO THE SCN PLACED IN GIRAFFE RADIANT WARMER AND EXPERIENCE HYPERTHERMIA DURING ADMISSION PROCESS. NOW WITH 2ND AND 3RD DEGREE BURN TO LOWER ABDOMEN, PERINEUM AND LEGS.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    577995 GIRAFFE INF WARMER GIRAFFE INF WARMER FMT GE HEALTHCARE 6650-0004-901

    Patients

    Seq Age Sex Outcome Treatment
    1 0 DA Required Intervention