BEUDAMED
    FDA Adverse Event Other Summary report: N

    SST BRAND TUBES

    MDR report key: 300844 · Received October 16, 2000

    Report

    Report Number
    1024879-2000-00026
    Event Type
    Other
    Date Received
    October 16, 2000
    Date of Event
    September 25, 2000
    Report Date
    October 16, 2000
    Manufacturer
    BECTON DICKINSON AND COMPANY
    Product Code
    JKA
    Removal / Correction Number
    NA
    Report Source
    Manufacturer report
    Reporter Location
    PA, US
    Reporter Occupation
    OTHER

    Narratives

    Description of Event or Problem · 1

    WHILE LABORATORY EMPLOYEE WAS DECAPPING TUBE (LOT NUMBER AND CATALOG NUMBER ARE UNKNOWN), TUBE BROKE AND CUT EMPLOYEE'S RIGHT THUMB. POST EXPOSURE TESTING PERFORMED AS PER HOSPITAL POLICY FOR HIV, HEP. C AND ALT.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 SST BRAND TUBES SST BRAND TUBES JKA BECTON DICKINSON AND COMPANY NA UNK

    Patients

    Seq Age Sex Outcome Treatment
    1 NA Other