BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    ARTHREX CAMERA

    MDR report key: 7212068 · Received January 22, 2018

    Report

    Report Number
    MW5074724
    Event Type
    Malfunction
    Date Received
    January 22, 2018
    Date of Event
    January 18, 2018
    Report Date
    January 19, 2018
    Manufacturer
    ARTHREX
    Product Code
    FWL
    Product Problem
    Yes
    Report Source
    Voluntary report
    Reporter Location
    CO, US
    Reporter Occupation
    OTHER HEALTH CARE PROFESSIONAL

    Narratives

    Description of Event or Problem · 1

    ARTHREX CAMERA WAS DARK ON SCREEN.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    55025 ARTHREX CAMERA ARTHREX CAMERA FWL ARTHREX

    Patients

    Seq Age Sex Outcome Treatment
    1 23 YR