BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    BD 25G X 1 INCH NEEDLE

    MDR report key: 23909869 · Received December 29, 2025

    Report

    Report Number
    MW5181332
    Event Type
    Malfunction
    Date Received
    December 29, 2025
    Date of Event
    December 19, 2025
    Report Date
    December 22, 2025
    Manufacturer
    BECTON DICKINSON AND COMPANY
    Product Code
    FMI
    Product Problem
    Yes
    Report Source
    Voluntary report
    Reporter Occupation
    PHARMACIST
    Health Professional
    Yes

    Narratives

    Description of Event or Problem · 0

    STAFF REPORTED DULL FEELING OF NEEDLE WHEN INJECTING PATIENTS. BD 25G X 1 INCH- REF 305761- LOT 5153197 BD 25G X 5/8 IN- REF 305759 LOT 5149514 BD NOTIFIED AND ARE IN PROCESS OF SHIPPING BACK TO MANUFACTURER. HEALTH EFFECT CODE: 4582. DEVICE PROBLEM CODE: 2407. REFERENCE REPORT: MW5181331.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    2706982 BD 25G X 1 INCH NEEDLE NEEDLE, HYPODERMIC, SINGLE LUMEN FMI BECTON DICKINSON AND COMPANY 305759 5149514

    Patients

    Seq Age Sex Outcome Treatment
    1 NA Unknown