BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    CONSTELLATION WITH LASER

    MDR report key: 2211681 · Received August 5, 2011

    Report

    Report Number
    2028159-2011-00889
    Event Type
    Malfunction
    Date Received
    August 5, 2011
    Date of Event
    July 2, 2011
    Report Date
    July 6, 2011
    Manufacturer
    ALCON - IRVINE TECHNOLOGY CENTER
    Product Code
    HQC
    PMA / PMN Number
    K063583
    Removal / Correction Number
    NA
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    FL, US
    Reporter Occupation
    NURSE

    Narratives

    Additional Manufacturer Narrative · 1

    INVESTIGATION INCLUDING ROOT CAUSE ANALYSIS IS IN PROGRESS. A SUPPLEMENTAL MDR WILL BE FILED AS NECESSARY IN ACCORDANCE WITH 21 CFR 803.56 WHEN ADDITIONAL REPORTABLE INFO BECOMES AVAILABLE. (B)(4).

    Description of Event or Problem · 1

    A CUSTOMER REPORTED THAT SYSTEM MESSAGE ERRORS DISPLAYED WHEN SWITCHING FROM FLUID TO GAS DURING A PROCEDURE. AN ALTERNATE SYSTEM WAS USED TO COMPLETE THE CASE. THERE WAS NO PT HARM REPORTED. THE CUSTOMER REFUSED TO PROVIDE ADDITIONAL INFO REGARDING THE EVENT.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 CONSTELLATION WITH LASER UNIT, PHACOFRAGMENTATION HQC ALCON - IRVINE TECHNOLOGY CENTER CONSTELLATION NA

    Patients

    Seq Age Sex Outcome Treatment
    1