BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    STERIDYNE

    MDR report key: 347174 · Received August 13, 2001

    Report

    Report Number
    MW1022618
    Event Type
    Malfunction
    Date Received
    August 13, 2001
    Date of Event
    June 11, 2001
    Report Date
    August 13, 2001
    Manufacturer
    STERIDYNE CORP
    Product Code
    FLL
    Product Problem
    Yes
    Report Source
    Voluntary report
    Reporter Location
    TX, US
    Reporter Occupation
    OTHER HEALTH CARE PROFESSIONAL

    Narratives

    Description of Event or Problem · 1

    THERMOMETER NOT READING TEMP CORRECTLY. REGISTERS BABY AS FEBRILE, ANOTHER SHOWS NO TEMP.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    36384 STERIDYNE DIGITAL THERMOMETER FLL STERIDYNE CORP VT-801 E 0012

    Patients

    Seq Age Sex Outcome Treatment
    1 * Other