BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    PHACOTRON GOLD

    MDR report key: 229686 · Received June 24, 1999

    Report

    Report Number
    2023366-1999-00025
    Event Type
    Malfunction
    Date Received
    June 24, 1999
    Report Date
    May 6, 1999
    Manufacturer
    CHIRON VISION CORP
    Product Code
    HQC
    Removal / Correction Number
    NA
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    OH, US
    Reporter Occupation
    OTHER

    Narratives

    Description of Event or Problem · 1

    THE PHACO LINEAR CONTROL WOULD NOT FUNCTION PROPERLY. PHACO POWER WOULD NOT FUNCTION PROPERLY UNLESS THE FOOTSWITCH WAS ENGAGED AND RE-ENGAGED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 PHACOTRON GOLD EQUIPMENT HQC CHIRON VISION CORP NA NA

    Patients

    Seq Age Sex Outcome Treatment
    1 UNKNOWN