BEUDAMED
    FDA Adverse Event Injury Summary report: N

    PLASTIPAK 3ML SYRINGE WITH BLUNT

    MDR report key: 21170124 · Received January 16, 2025

    Report

    Report Number
    MW5164834
    Event Type
    Injury
    Date Received
    January 16, 2025
    Date of Event
    January 10, 2025
    Report Date
    January 13, 2025
    Manufacturer
    BECTON, DICKINSON AND COMPANY
    Product Code
    FMF
    Product Problem
    Yes
    Report Source
    Voluntary report
    Reporter Location
    OK, US
    Reporter Occupation
    PHARMACIST
    Health Professional
    Yes

    Narratives

    Description of Event or Problem · 0

    SOLU-MEDROL 40MG/VIAL AND SOLU-MEDROL 125MG/VIAL WHEN DRAWN UP WITH A BECTON, DICKINSON AND COMPANY PLASTIPAK 3ML SYRINGE WITH BLUNT FILL NEEDLE CREATES A CORE IN THE VIAL OR SYRINGE. MULTIPLE EXAMPLES.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1056598 PLASTIPAK 3ML SYRINGE WITH BLUNT SYRINGE, PISTON FMF BECTON, DICKINSON AND COMPANY 305060 4277741

    Patients

    Seq Age Sex Outcome Treatment
    1 NA Unknown Required Intervention SOLU-MEDROL 40MG/VIAL ACTOVIAL.