BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    SYBRONENDO

    MDR report key: 8182700 · Received December 19, 2018

    Report

    Report Number
    2016150-2018-00062
    Event Type
    Malfunction
    Date Received
    December 19, 2018
    Report Date
    December 18, 2018
    Manufacturer
    SYBRONENDO
    Product Code
    EKZ
    PMA / PMN Number
    K031664
    Removal / Correction Number
    Z-0413-2018
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    WA, US
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 1

    THE PRODUCT HAS BEEN IDENTIFIED AS A POTENTIAL AFFECTED PRODUCT IN AN ONGOING CLASS II RECALL; THEREFORE NO FURTHER EVALUATION IS NECESSARY.

    Description of Event or Problem · 1

    A COMPLAINANT ALLEGED UNIT GOT REALLY HOT AND BURNED THE DOCTORS THUMB.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1021717 SYBRONENDO ELEMENTS OBTURATION UNIT EKZ SYBRONENDO

    Patients

    Seq Age Sex Outcome Treatment
    1