BEUDAMED
    FDA Adverse Event Other Summary report: N

    SST BRAND TUBES

    MDR report key: 300846 · Received October 16, 2000

    Report

    Report Number
    1024879-2000-00027
    Event Type
    Other
    Date Received
    October 16, 2000
    Date of Event
    September 11, 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 DECAPPING TUBE (LOT NUMBER AND CATALOG NUMBER UNKNOWN), TUBE BROKE AND EMPLOYEE RECEIVED A CUT TO 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