BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    N/A

    MDR report key: 22352634 · Received June 30, 2025

    Report

    Report Number
    22352634
    Event Type
    Malfunction
    Date Received
    June 30, 2025
    Date of Event
    May 25, 2025
    Report Date
    June 25, 2025
    Manufacturer
    BECTON, DICKINSON AND COMPANY
    Product Code
    GAA
    UDI-DI
    00382903051809
    Product Problem
    Yes
    Report Source
    User Facility report
    Reporter Location
    VA
    Reporter Occupation
    RISK MANAGER
    Health Professional
    N

    Narratives

    Description of Event or Problem · 0

    ONE OF OUR NURSES WAS PULLING UP MEDICATIONS OUT OF A TORADOL VIAL. SHE WAS HAVING A LITTLE BIT OF DIFFICULTY DRAWING UP THE MED, SO SHE TRIED TO PULL THE NEEDLE OUT. WHEN SHE DID THAT THE RED PORTION OF THE BLUNT NEEDLE, IT'S THE BD BLUNT FILLED NEEDLE 18 G 1-1.5 INCH NEEDLES, THE RED PART CAME OFF AND LEFT THE NEEDLE INSIDE OF THE VIAL. LOT NUMBER 5002107 EXP 02-29-2030 IT'S THE BD BLUNT FILLED NEEDLE 18 G 1-1.5 INCH THE NEEDLE CAME OFF FROM THE RED PORTION OF THE BLUNT NEEDLE AND IT STAYED IN THE VIAL.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    969955 N/A NEEDLE, ASPIRATION AND INJECTION, DISPOSABLE GAA BECTON, DICKINSON AND COMPANY 305180 5002107 00382903051809

    Patients

    Seq Age Sex Outcome Treatment
    1 NA Unknown