BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    DIGITAL RADIOGRAPHY CXDI-50G

    MDR report key: 2897057 · Received December 31, 2012

    Report

    Report Number
    1000181430-2012-00098
    Event Type
    Malfunction
    Date Received
    December 31, 2012
    Report Date
    March 18, 2010
    Manufacturer
    CANON, INC.
    Product Code
    MQB
    PMA / PMN Number
    K031447
    Removal / Correction Number
    NA
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    MA, US
    Reporter Occupation
    NOT APPLICABLE

    Narratives

    Additional Manufacturer Narrative · 1

    THIS MDR IS BEING SUBMITTED RETROACTIVELY AS A RESULT OF AN INTERNAL AUDIT OF COMPLAINT FILES CONDUCTED BY (B)(4). THE PRODUCT WAS RETURNED FOR EVALUATION. THE SERVICE ENGINEER REPLACED THE A/D AND LED PC BOARDS. ALL FUNCTIONS WERE CHECKED AND MET SPECIFICATIONS. (B)(4).

    Description of Event or Problem · 1

    THE CUSTOMER REPORTED THAT AN ERROR CODE DISPLAYED ON THE SYSTEM. IT IS POSSIBLE THAT THE IMAGE WAS RETAKEN, RESULTING IN UNINTENDED RADIATION EXPOSURE.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 DIGITAL RADIOGRAPHY CXDI-50G MQB CANON, INC. CDXI-50G NA

    Patients

    Seq Age Sex Outcome Treatment
    1 UNK