BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    CAPTURE-R READY INDICATOR RED CELLS

    MDR report key: 6220063 · Received January 3, 2017

    Report

    Report Number
    1034569-2017-00006
    Event Type
    Malfunction
    Date Received
    January 3, 2017
    Date of Event
    November 22, 2016
    Report Date
    January 3, 2017
    Manufacturer
    IMMUCOR, INC.
    Product Code
    KSF
    UDI-DI
    10888234000600
    PMA / PMN Number
    BK020053
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    VA, US
    Reporter Occupation
    MEDICAL TECHNOLOGIST

    Narratives

    Additional Manufacturer Narrative · 1

    THE FULL NUMBER FOR THE PRODUCT IN QUESTION IS BK020053 (1/27/2003). IMMUCOR TECHNICAL SUPPORT PERFORMED A DHR REVIEW BECAUSE THE PRODUCT HAD ALREADY EXPIRED, WHICH SHOWED THAT ALL SPECIFICATIONS HAD BEEN MET PRIOR TO RELEASE OF THE PRODUCT TO THE MARKET.

    Description of Event or Problem · 1

    ON (B)(6) 2016, A CUSTOMER REPORTED AN UNEXPECTED NEGATIVE ANTIBODY SCREEN WHEN USING CAPTURE-R READY INDICATOR RED CELLS ON A GALILEO ECHO INSTRUMENT.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    2320 CAPTURE-R READY INDICATOR RED CELLS ANTIGLOBULIN COATED RED CELLS KSF IMMUCOR, INC. 221753 10888234000600

    Patients

    Seq Age Sex Outcome Treatment
    1 51 YR