BEUDAMED
    FDA Adverse Event Other Summary report: N

    2.7ML, LT. BLUE CONVENTIONAL GLASS, NACITRATE

    MDR report key: 293577 · Received August 30, 2000

    Report

    Report Number
    1917413-2000-00019
    Event Type
    Other
    Date Received
    August 30, 2000
    Date of Event
    August 9, 2000
    Report Date
    August 30, 2000
    Manufacturer
    BECTON DICKINSON AND COMPANY
    Product Code
    JKA
    Removal / Correction Number
    NA
    Report Source
    Manufacturer report
    Reporter Location
    LA, US
    Reporter Occupation
    OTHER

    Narratives

    Description of Event or Problem · 1

    APPROX 20 TUBES BROKE DURING CENTRIFUGATION. OTHERS BROKE, FURTHER, WHILE TRYING TO REMOVE CAP, RESULTING IN A TECH CUTTING TECH'S FINGER. FIRST AID WAS ADMINISTERED, BODY FLUIDS ARE UNKNOWN TO BE INFECTIOUS.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 2.7ML, LT. BLUE CONVENTIONAL GLASS, NACITRATE CITRATE TUBES JKA BECTON DICKINSON AND COMPANY NA 0046894

    Patients

    Seq Age Sex Outcome Treatment
    1 NA Other