BEUDAMED
    FDA Adverse Event Other Summary report: N

    BD GOLD HEMOGUARD VACUTAINER

    MDR report key: 103789 · Received June 30, 1997

    Report

    Report Number
    103789
    Event Type
    Other
    Date Received
    June 30, 1997
    Date of Event
    December 13, 1996
    Report Date
    February 10, 1997
    Manufacturer
    BECTON DICKINSON/VACUTAINER SYSTEMS
    Product Code
    JKA
    Adverse Event
    Yes
    Product Problem
    Yes
    Report Source
    User Facility report
    Reporter Location
    PA, US
    Reporter Occupation
    OTHER

    Narratives

    Description of Event or Problem · 1

    LAB TECHNICIAN REMOVED CAP OFF OF BD GOLD HEMOTOP TUBE. GLASS TUBE WAS BROKEN AROUND RIM UNDERNEATH CAP. SOME GLASS REMAINED ATTACHED TO THE CAP AND TUBE HAD JAGGED EDGE. TECHNICIAN CUT LEFT THUMB ON GLASS ATTACHED TO CAP. SPECIMEN WAS FROM HIV+ PT.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 BD GOLD HEMOGUARD VACUTAINER TEST TUBE JKA BECTON DICKINSON/VACUTAINER SYSTEMS * 616356

    Patients

    Seq Age Sex Outcome Treatment
    1 NO INFO Other