BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    BD SAFETY GLIDE NEEDLE 25GAUGE X1INCH TW

    MDR report key: 24034009 · Received January 12, 2026

    Report

    Report Number
    MW5182025
    Event Type
    Malfunction
    Date Received
    January 12, 2026
    Date of Event
    January 5, 2026
    Report Date
    January 5, 2026
    Manufacturer
    BECTON DICKINSON AND COMPANY
    Product Code
    FMI
    Product Problem
    Yes
    Report Source
    Voluntary report
    Reporter Location
    PA, US
    Reporter Occupation
    RISK MANAGER
    Health Professional
    Yes

    Narratives

    Description of Event or Problem · 0

    NEEDLE DETACHED FROM SYRINGE AND REMAINED IN PATIENTS ARM. REMOVED INTACT NEEDLE WITHOUT DIFFICULTY. BD SAFETY GLIDE NEEDLE 25GAUGE X1INCH TW, LOT# 5233985, EXPIRATION 07/31/2030, REFERENCE # (B)(4).

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    107783 BD SAFETY GLIDE NEEDLE 25GAUGE X1INCH TW NEEDLE, HYPODERMIC, SINGLE LUMEN FMI BECTON DICKINSON AND COMPANY 305916 5233985

    Patients

    Seq Age Sex Outcome Treatment
    1 71 YR Female