BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    ALARIS

    MDR report key: 25315620 · Received May 28, 2026

    Report

    Report Number
    25315620
    Event Type
    Malfunction
    Date Received
    May 28, 2026
    Date of Event
    April 26, 2026
    Report Date
    May 27, 2026
    Manufacturer
    BD SWITZERLAND SÀRL
    Product Code
    FPA
    Product Problem
    Yes
    Report Source
    User Facility report
    Reporter Location
    UT
    Reporter Occupation
    003

    Narratives

    Description of Event or Problem · 0

    NOTICED A 1.5-2CM AIR BUBBLE IN THE LINE FOR PT W/ IV RUNNING D10 SPN [SUPPLEMENTAL PARENTERAL NUTRITION] WITH HEPARIN WOULDN'T CLEAR- BAD TUBING.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    132287 ALARIS SET, ADMINISTRATION, INTRAVASCULAR FPA BD SWITZERLAND SÀRL 2202-0007 23095114

    Patients

    Seq Age Sex Outcome Treatment
    1 NA Male Other