BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    3ML, 5ML, AND 10ML SYRINGES

    MDR report key: 20556320 · Received October 29, 2024

    Report

    Report Number
    20556320
    Event Type
    Malfunction
    Date Received
    October 29, 2024
    Date of Event
    October 1, 2024
    Report Date
    October 4, 2024
    Manufacturer
    BECTON DICKINSON
    Product Code
    FMF
    Product Problem
    Yes
    Report Source
    User Facility report
    Reporter Location
    PA
    Reporter Occupation
    OTHER HEALTH CARE PROFESSIONAL
    Health Professional
    Yes

    Narratives

    Description of Event or Problem · 0

    3, 5, AND 10ML SYRINGES MADE MY BECTON, DICKINSON AND COMPANY WHEN USED WITH 25, 23, AND 18G NEEDLES MADE BY SMITHS MEDICAL ASD, INC. ARE NOT STRAIGHT AND CROOKED. 3ML SYRINGE LOT 0261806. 5ML SYRINGE LOT 0262024. 10ML SYRINGE LOT 3300611. 25G 5/8" NEEDLE LOT 4459972. 23G 1" NEEDLE LOT 4378190. 18G 1.5" NEEDLE LOT 6028657.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    321106 3ML, 5ML, AND 10ML SYRINGES SYRINGE, PISTON FMF BECTON DICKINSON 0261806, 0262024, 3300611

    Patients

    Seq Age Sex Outcome Treatment
    1 NA Unknown