BEUDAMED
    FDA Adverse Event Other Summary report: N

    VACUTAINER BRAND TUBE, 7 ML CONVENTIONAL PLAIN RED

    MDR report key: 274261 · Received April 17, 2000

    Report

    Report Number
    1024879-2000-00013
    Event Type
    Other
    Date Received
    April 17, 2000
    Date of Event
    March 22, 2000
    Report Date
    April 17, 2000
    Manufacturer
    BECTON DICKINSON AND COMPANY
    Product Code
    JKA
    Removal / Correction Number
    NA
    Report Source
    Manufacturer report
    Reporter Location
    KS
    Reporter Occupation
    OTHER

    Narratives

    Description of Event or Problem · 1

    TUBE BROKE IN HAND OF TECH DURING BLOOD TESTING. BODY FLUIDS WERE NOT INFECTIOUS AND TECH ONLY REQUIRED CLEANSING OF WOUND WITH NO MEDICAL INTERVENTION.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 VACUTAINER BRAND TUBE, 7 ML CONVENTIONAL PLAIN RED VACUTAINER BRAND TUBE, SERUM, PLAIN RED TOP JKA BECTON DICKINSON AND COMPANY NA 9J710

    Patients

    Seq Age Sex Outcome Treatment
    1 NA Other