BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    N/A

    MDR report key: 23592860 · Received November 19, 2025

    Report

    Report Number
    23592860
    Event Type
    Malfunction
    Date Received
    November 19, 2025
    Date of Event
    September 5, 2025
    Report Date
    September 22, 2025
    Manufacturer
    BECTON, DICKINSON AND COMPANY
    Product Code
    GAA
    Product Problem
    Yes
    Report Source
    User Facility report
    Reporter Location
    MI
    Reporter Occupation
    RISK MANAGER
    Health Professional
    N

    Narratives

    Description of Event or Problem · 0

    TOOK BD BLUNT FILL NEEDLE OUT OF PACKAGING AND FOUND WHITE BUILDUP ON NEEDLE PRIOR TO USE. PRODUCT WORKDAY ITM-NUMBER: (B)(4). LOT NUMBER: 5092742. SUPPLIER & SUPPLIER REFERENCE/RE-ORDER OR ITEM NUMBER: BD. REF: 305180. EXPIRATION DATE: 2030-05-31.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    2859888 N/A NEEDLE, ASPIRATION AND INJECTION, DISPOSABLE GAA BECTON, DICKINSON AND COMPANY 305180 5092742

    Patients

    Seq Age Sex Outcome Treatment
    1 NA Unknown