BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    GALILEO ECHO

    MDR report key: 3895248 · Received June 25, 2014

    Report

    Report Number
    1034569-2014-00107
    Event Type
    Malfunction
    Date Received
    June 25, 2014
    Date of Event
    May 12, 2014
    Report Date
    June 25, 2014
    Manufacturer
    IMMUCOR, INC.
    Product Code
    KSZ
    PMA / PMN Number
    BK070016
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    NJ, US
    Reporter Occupation
    MEDICAL TECHNOLOGIST

    Narratives

    Additional Manufacturer Narrative · 1

    IMMUCOR TECHNICAL SUPPORT ASSESSED INSTRUMENT WELL IMAGES VIA A REMOTE ELECTRONIC CONNECTION METHOD ON (B)(4) 2014, BY VIEWING ARCHIVED RESULTS ON AN ARCHIVE DISK.

    Description of Event or Problem · 1

    ON (B)(6) 2014, A CUSTOMER REPORTED UNEXPECTED NEGATIVE ANTIBODY SCREEN WHEN USING CAPTURE-R READY-SCREEN (3) ON A GALILEO ECHO INSTRUMENT ON (B)(6) 2014.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    371956 GALILEO ECHO AUTOMATED BLOOD BANK SYSTEM KSZ IMMUCOR, INC.

    Patients

    Seq Age Sex Outcome Treatment
    1 26 YR