BEUDAMED
    FDA Adverse Event Other Summary report: N

    BD

    MDR report key: 2423777 · Received January 16, 2012

    Report

    Report Number
    MW5023866
    Event Type
    Other
    Date Received
    January 16, 2012
    Date of Event
    January 16, 2012
    Report Date
    January 16, 2012
    Manufacturer
    BECTON DICKINSON AND CO.
    Product Code
    FMI
    Adverse Event
    Yes
    Report Source
    Voluntary report
    Reporter Location
    MI, US
    Reporter Occupation
    NURSE

    Narratives

    Description of Event or Problem · 1

    SURGICAL RESIDENT UNCAPPED NEEDLE AND GRAZED HER LEFT INDEX FINGER WITH TIP OF CONTAMINATED NEEDLE. SHE NEEDED TO HAVE A TETANUS INJECTION DUE TO THIS INJURY.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 BD PRECISION GLIDE NEEDLE WITHOUT SAFETY DEVICE FMI BECTON DICKINSON AND CO. 305127

    Patients

    Seq Age Sex Outcome Treatment
    1 31 YR Other