BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    SWABCAP

    MDR report key: 20406456 · Received October 9, 2024

    Report

    Report Number
    20406456
    Event Type
    Malfunction
    Date Received
    October 9, 2024
    Date of Event
    October 4, 2024
    Report Date
    October 7, 2024
    Manufacturer
    ICU MEDICAL, INC.
    Product Code
    QBP
    Product Problem
    Yes
    Report Source
    User Facility report
    Reporter Location
    CA
    Reporter Occupation
    RISK MANAGER
    Health Professional
    N

    Narratives

    Description of Event or Problem · 0

    ICU MEDICAL SWABCAPS ARE DRY UPON OPENING.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    729628 SWABCAP CAP, DEVICE DISINFECTANT QBP ICU MEDICAL, INC. SCRC3-10-1600 13837606

    Patients

    Seq Age Sex Outcome Treatment
    1 NA Prefer Not To Disclose