BEUDAMED
    FDA Adverse Event Injury Summary report: N

    XRAY CAMERA

    MDR report key: 14575727 · Received June 1, 2022

    Report

    Report Number
    MW5110044
    Event Type
    Injury
    Date Received
    June 1, 2022
    Date of Event
    May 28, 2022
    Report Date
    May 28, 2022
    Manufacturer
    CANON INC.
    Product Code
    MQB
    Adverse Event
    Yes
    Product Problem
    Yes
    Report Source
    Voluntary report
    Reporter Location
    WA, US
    Reporter Occupation
    PATIENT
    Health Professional
    *

    Narratives

    Description of Event or Problem · 0

    HAIR LOSS AND DENTAL AND EYE; NEIGHBORS XRAY AND THERMAL CAMERAS. UNLICENSED DEVICES AND COMING FROM 2 DIRECTIONS. CAUSES SEVERE EYES STRAIN BUT RADIATION WAVES ARE VISIBLE. AREA IS NOT ZONED FOR HOSPITAL ACTIVITIES AND EQUIPMENT IS UNLICENSED. HOUSED IN TWO ADJACENT HOMES. FDA SAFETY REPORT ID # (B)(4).

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    22566 XRAY CAMERA SOLID STATE X-RAY IMAGER (FLAT PANEL/DIGITAL IMAGER) MQB CANON INC.

    Patients

    Seq Age Sex Outcome Treatment
    1 47 YR Male Other| L| S| R