BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    ACCELERATOR APS CENTRIFUGE MODULE

    MDR report key: 1171500 · Received September 17, 2008

    Report

    Report Number
    1628664-2008-00209
    Event Type
    Malfunction
    Date Received
    September 17, 2008
    Report Date
    August 6, 2008
    Manufacturer
    ABBOTT MANUFACTURING, INC.
    Product Code
    JQP
    PMA / PMN Number
    EXEMPT
    Removal / Correction Number
    1628664-09/10/08-002-C
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    IL, US
    Reporter Occupation
    OTHER

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 ACCELERATOR APS CENTRIFUGE MODULE CENTRIFUGE MODULE FOR AUTOMATED SAMPLE HANDLING AND PROCESSING SYSTEM JQP ABBOTT MANUFACTURING, INC. NA NA

    Patients

    Seq Age Sex Outcome Treatment
    1 NI