BEUDAMED
    FDA Adverse Event Injury Summary report: N

    BD BLUNT FILL NEEDLE

    MDR report key: 23871623 · Received December 22, 2025

    Report

    Report Number
    MW5180994
    Event Type
    Injury
    Date Received
    December 22, 2025
    Date of Event
    December 14, 2025
    Report Date
    December 15, 2025
    Manufacturer
    BECTON DICKINSON
    Product Code
    GAA
    Adverse Event
    Yes
    Product Problem
    Yes
    Report Source
    Voluntary report
    Reporter Location
    CA, US
    Reporter Occupation
    UNKNOWN
    Health Professional
    *

    Narratives

    Description of Event or Problem · 0

    BLUNT FILL NEEDLE, LOT #5092740, REF # 305180, WHICH WAS IN USE IN THE MEDICATION ROOM ON (B)(6). AN EMPLOYEE REPORTED THAT THE BLUNT FILL NEEDLE APPEARED SHARPER THAN USUAL DURING MEDICATION PREPARATION, RAISING CONCERN FOR A POTENTIAL EQUIPMENT-RELATED ISSUE AND DIRECTLY CAUSING AN EMPLOYEE INJURY.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    2696110 BD BLUNT FILL NEEDLE NEEDLE, ASPIRATION AND INJECTION, DISPOSABLE GAA BECTON DICKINSON 5092740

    Patients

    Seq Age Sex Outcome Treatment
    1 NA Unknown