BEUDAMED
    FDA Adverse Event Injury Summary report: N

    SINGLE USE NEBULIZER WITH TUBING

    MDR report key: 8074750 · Received November 14, 2018

    Report

    Report Number
    MW5081314
    Event Type
    Injury
    Date Received
    November 14, 2018
    Date of Event
    October 16, 2018
    Report Date
    November 10, 2018
    Manufacturer
    ALLIED HEALTHCARE PRODUCTS, INC. AS B & F MEDICAL
    Product Code
    CAF
    Product Problem
    Yes
    Report Source
    Voluntary report
    Reporter Location
    NY, US
    Reporter Occupation
    OTHER HEALTH CARE PROFESSIONAL

    Narratives

    Description of Event or Problem · 1

    OXYGEN TUBING WOULD NOT STAY CONNECTED TO NEBULIZER UNDER PRESSURE. THE FITTING AT THE END OF THE TUBING DID NOT APPEAR TO FIT THE NEBULIZER CORRECTLY. THE TUBING REPEATEDLY POPPED OFF DURING PATIENT CARE, THE EMT IN CHARGE HAD TO TAPE THE TUBING IN PLACE. THE POOR FIT WAS VERIFIED BY OTHER EMT'S.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    907747 SINGLE USE NEBULIZER WITH TUBING NEBULIZER (DIRECT PATIENT INTERFACE) CAF ALLIED HEALTHCARE PRODUCTS, INC. AS B & F MEDICAL 64085 VARIOUS

    Patients

    Seq Age Sex Outcome Treatment
    1 Required Intervention