BEUDAMED
    FDA Adverse Event Other Summary report: N

    SMARTSITE LOW SORBING EXTENSION SET 0.2 FILTER

    MDR report key: 24887705 · Received April 15, 2026

    Report

    Report Number
    MW5186853
    Event Type
    Other
    Date Received
    April 15, 2026
    Date of Event
    April 10, 2026
    Report Date
    April 10, 2026
    Manufacturer
    BD (BECTON, DICKINSON AND COMPANY)/CAREFUSION 2200, INC.
    Product Code
    FPA
    Report Source
    Voluntary report
    Reporter Location
    NY, US
    Reporter Occupation
    PHARMACIST
    Health Professional
    *

    Narratives

    Description of Event or Problem · 0

    A 0.2 BD FILTER CLOGGED AGAIN AFTER CHANGING OUT THE FIRST CLOGGED FILTER. PT: 4582. DEVICE: 2423, 2588. REF: MW5186852.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    948863 SMARTSITE LOW SORBING EXTENSION SET 0.2 FILTER SET, ADMINISTRATION, INTRAVASCULAR FPA BD (BECTON, DICKINSON AND COMPANY)/CAREFUSION 2200, INC.

    Patients

    Seq Age Sex Outcome Treatment
    1 NA Female