BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    DIGITAL RADIOGRAPHY CXDI-55C

    MDR report key: 2897134 · Received December 31, 2012

    Report

    Report Number
    1000181430-2012-00146
    Event Type
    Malfunction
    Date Received
    December 31, 2012
    Report Date
    April 27, 2011
    Manufacturer
    CANON, INC
    Product Code
    MQB
    PMA / PMN Number
    K091436
    Removal / Correction Number
    NA
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    CT, 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 CANON HEALTHCARE SOLUTIONS USA. (B)(4). THE SERVICE REP FOUND THAT THE CONNECTION TO THE DI BOARD WAS LOOSE. HE REPLACED THE SIDE COVERS AND CENTER FRICTION PAD. THE SYSTEM WAS RETESTED AND PASSED ALL TESTS. (B)(4).

    Description of Event or Problem · 1

    THE CUSTOMER WAS EXPERIENCING INTERMITTENT ERROR MESSAGES, INCLUDING AN "IMAGE READ ERROR" IMAGES. 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-55C MQB CANON, INC CXDI-55C NA

    Patients

    Seq Age Sex Outcome Treatment
    1 UNK