BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    ALARIS

    MDR report key: 20189312 · Received September 11, 2024

    Report

    Report Number
    20189312
    Event Type
    Malfunction
    Date Received
    September 11, 2024
    Date of Event
    April 10, 2024
    Report Date
    April 10, 2024
    Manufacturer
    BD SWITZERLAND SÀRL
    Product Code
    FPA
    UDI-DI
    07613203012591
    Product Problem
    Yes
    Report Source
    User Facility report
    Reporter Location
    VA
    Reporter Occupation
    RISK MANAGER
    Health Professional
    N

    Narratives

    Description of Event or Problem · 0

    IVIG TUBING VERY HARD TO PRIME. HAVE HAD THIS HAPPEN MULTIPLE TIMES.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    556550 ALARIS SET, ADMINISTRATION, INTRAVASCULAR FPA BD SWITZERLAND SÀRL 2260-0500 (10)23126253 07613203012591

    Patients

    Seq Age Sex Outcome Treatment
    1 NA Unknown