BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    DIGITAL RETINAL CAMERA CX-1

    MDR report key: 2980347 · Received January 28, 2013

    Report

    Report Number
    1000181430-2013-00027
    Event Type
    Malfunction
    Date Received
    January 28, 2013
    Report Date
    January 17, 2012
    Manufacturer
    CANON INC.
    Product Code
    NFJ
    PMA / PMN Number
    K092565
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    PA, US
    Reporter Occupation
    PHYSICIAN

    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 ENGINEER COULD NOT VERIFY THE PROBLEM DURING THE SERVICE EVALUATION. HE REPLACED THE MOTOR ON THE MYD/NON MYD FILTER. HE RETESTED THE SYSTEM AND THE PERFORMANCE WAS OK. (B)(4).

    Description of Event or Problem · 1

    THE CUSTOMER REPORTED THAT THERE WAS AN ARTIFACT IN THE IMAGES. PART OF THE LEFT SIDE OF THE IMAGE WAS DARK. THIS PROBLEM APPEARS INTERMITTENTLY. NO INFORMATION WAS PROVIDED REGARDING WHAT IMAGE TYPES (COLOR, RED-FREE, FLUORESCEIN ANGIOGRAPHY) WERE AFFECTED. THE CUSTOMER DID NOT STATE THAT THE FLUORESCEIN IMAGING WAS REPEATED. HOWEVER, IF THE PROBLEM OCCURRED DURING THE FLUORESCEIN IMAGING PORTION OF THE EXAM, THE TECHNICIAN MAY HAVE RESCHEDULED THE EXAM. A RESCHEDULED EXAM WOULD HAVE INVOLVED A REPEAT INJECTION OF FLUORESCEIN.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    38364 DIGITAL RETINAL CAMERA CX-1 NFJ CANON INC. CX-1 NA

    Patients

    Seq Age Sex Outcome Treatment
    1 UNK