BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    POSIFLUSH

    MDR report key: 24925899 · Received April 20, 2026

    Report

    Report Number
    1911916-2026-00181
    Event Type
    Malfunction
    Date Received
    April 20, 2026
    Date of Event
    March 20, 2026
    Report Date
    May 12, 2026
    Manufacturer
    BD MEDICAL (BD WEST) MEDICAL SURGICAL
    Product Code
    NGT
    UDI-DI
    00382903065462
    PMA / PMN Number
    K003553
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    IL, US
    Reporter Occupation
    OTHER HEALTH CARE PROFESSIONAL
    Health Professional
    Yes

    Narratives

    Additional Manufacturer Narrative · 0

    H.3. A DEVICE EVALUATION AND/OR DEVICE HISTORY REVIEW IS ANTICIPATED BUT IS NOT COMPLETE. UPON COMPLETION, A SUPPLEMENTAL REPORT WILL BE FILED. G.4. ADDITIONAL 510K: K141311, K250884.

    Description of Event or Problem · 0

    IT IS REPORTED, SOLUTION INSIDE IS VERY CLOUDY AND DOESN¿T LOOK LIKE NS EITHER.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    496872 POSIFLUSH SET, ADMINISTRATION, INTRAVASCULAR NGT BD MEDICAL (BD WEST) MEDICAL SURGICAL 5218133 00382903065462

    Patients

    Seq Age Sex Outcome Treatment
    1 NA Unknown