BEUDAMED
    FDA Adverse Event Injury Summary report: N

    BD INSULIN SYRINGE/ULTRA FINE NEEDLE 310 8MM 31G

    MDR report key: 3802991 · Received May 4, 2014

    Report

    Report Number
    MW5035952
    Event Type
    Injury
    Date Received
    May 4, 2014
    Date of Event
    February 10, 2014
    Report Date
    May 4, 2014
    Manufacturer
    BD
    Product Code
    FMF
    Product Problem
    Yes
    Report Source
    Voluntary report
    Reporter Location
    OH, US
    Reporter Occupation
    PHARMACIST

    Narratives

    Description of Event or Problem · 1

    INSULIN SYRINGE NEEDLE LOOKS AS THOUGH THERE ARE GROOVES ETCHED INTO THE NEEDLE CAUSING "DRAG" WHEN INJECTING. PAINFUL TO USE. ALSO, RUBBER STOPPER INSIDE SYRINGE APPEARS TO HAVE MOISTURE LOCKED INSIDE. DOSE OR AMOUNT: 100 SYRINGE, FREQUENCY: ONCE DAILY, ROUTE: SUBCUTANEOUS. REASON FOR USE: DIABETES MELLITUS.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    266147 BD INSULIN SYRINGE/ULTRA FINE NEEDLE 310 8MM 31G SYRINGE FMF BD UNKNOWN

    Patients

    Seq Age Sex Outcome Treatment
    1 11 YR Required Intervention