BEUDAMED
    FDA Adverse Event Other Summary report: N

    VAPOTHERM

    MDR report key: 18536262 · Received January 17, 2024

    Report

    Report Number
    MW5150486
    Event Type
    Other
    Date Received
    January 17, 2024
    Date of Event
    November 23, 2023
    Report Date
    January 12, 2024
    Manufacturer
    VAPOTHERM, INC.
    Product Code
    CAN
    Report Source
    Voluntary report
    Reporter Occupation
    RISK MANAGER
    Health Professional
    Yes

    Narratives

    Description of Event or Problem · 0

    VAPOTHERM FLOW TURNED OFF. FIO2 AND WATER TEMP REMAINED ON.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    2065330 VAPOTHERM REGULATOR, PRESSURE, GAS CYLINDER CAN VAPOTHERM, INC.

    Patients

    Seq Age Sex Outcome Treatment
    1 10 DA Male