BEUDAMED
    FDA Adverse Event Injury Summary report: N

    BD PRECISION GLIDE 22G 1 INCH NEEDLE

    MDR report key: 2163632 · Received July 11, 2011

    Report

    Report Number
    MW5021331
    Event Type
    Injury
    Date Received
    July 11, 2011
    Date of Event
    July 11, 2011
    Report Date
    July 11, 2011
    Manufacturer
    BD
    Product Code
    FMI
    Adverse Event
    Yes
    Report Source
    Voluntary report
    Reporter Location
    MI, US
    Reporter Occupation
    NURSE

    Narratives

    Description of Event or Problem · 1

    RESPIRATORY THERAPIST WAS HOLDING PT'S HAND WHILE THE OTHER RESPIRATORY THERAPIST WAS DRAWING ABG'S, THE RT DRAWING WITHDREW THE NEEDLE TO RE-ADJUST AND POKED THE EMPLOYEE IN THE LEFT LITTLE FINGER. I HAD TO GIVE THE INJURED EMPLOYEE A 0.5ML TDAP DUE TO THE INJURY.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 BD PRECISION GLIDE 22G 1 INCH NEEDLE ABG NEEDLE FMI BD 301695

    Patients

    Seq Age Sex Outcome Treatment
    1 25 YR Other