BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    NEO THERM

    MDR report key: 248445 · Received November 3, 1999

    Report

    Report Number
    MW1017461
    Event Type
    Malfunction
    Date Received
    November 3, 1999
    Date of Event
    September 27, 1999
    Report Date
    November 2, 1999
    Manufacturer
    RESPIRATORY SUPPORT PRODUCTS, INC.
    Product Code
    FLL
    Product Problem
    Yes
    Report Source
    Voluntary report
    Reporter Location
    TX, US
    Reporter Occupation
    OTHER

    Narratives

    Description of Event or Problem · 1

    TEMPERATURE PROBE WOULD NOT WORK.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 NEO THERM SKIN TEMPERATURE SENSOR FLL RESPIRATORY SUPPORT PRODUCTS, INC. NA 1614

    Patients

    Seq Age Sex Outcome Treatment
    1 * Other