BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    SYR BD NED U-FINE 1ML 30G 1/2

    MDR report key: 2651068 · Received July 3, 2012

    Report

    Report Number
    MW5026091
    Event Type
    Malfunction
    Date Received
    July 3, 2012
    Date of Event
    June 19, 2012
    Report Date
    June 26, 2012
    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

    SYR BD NED U-FINE 1 ML 30 G 1/2 CONTAINING 9 PACK OF SYRINGES HAD 3 PACKS CONTAINING 0.5 ML SYRINGES INSTEAD OF 1 ML SYRINGES. INJECTIONS FOUR TIMES A DAY. DIAGNOSIS FOR USE: DIABETES.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 SYR BD NED U-FINE 1ML 30G 1/2 SYRINGE/NEEDLE FMF BD 2030752

    Patients

    Seq Age Sex Outcome Treatment
    1 77 YR