BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    BECKMAN J2-21

    MDR report key: 102078 · Received June 24, 1997

    Report

    Report Number
    2912312-1997-00001
    Event Type
    Malfunction
    Date Received
    June 24, 1997
    Date of Event
    June 4, 1997
    Report Date
    June 23, 1997
    Manufacturer
    BECKMAN INSTRUMENTS, INC.
    Product Code
    JQC
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    PA, US
    Reporter Occupation
    OTHER

    Narratives

    Description of Event or Problem · 1

    CUSTOMER WAS OPENING THE LID ON A J2-21 CENTRIFUGE, THE GAS FILLED SUPPORT ARMS "SPRINGS" FAILED TO HOLD THE DOOR OPEN. THE LID FELL ON THE USER'S SHOULDER CAUSING BRUISING.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 BECKMAN J2-21 CENTRIFUGE JQC BECKMAN INSTRUMENTS, INC. J2-21 NA

    Patients

    Seq Age Sex Outcome Treatment
    1 * Other