BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    CROSSFIRE FOOTSWITCH

    MDR report key: 2050063 · Received April 4, 2011

    Report

    Report Number
    2936485-2011-00197
    Event Type
    Malfunction
    Date Received
    April 4, 2011
    Date of Event
    March 9, 2011
    Report Date
    March 9, 2011
    Manufacturer
    STRYKER ENDOSCOPY SAN JOSE
    Product Code
    GEI
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    IL, US
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 1

    ADDITIONAL INFORMATION WILL BE PROVIDED ONCE THE INVESTIGATION HAS BEEN COMPLETED.

    Description of Event or Problem · 1

    IT WAS REPORTED THAT WHEN USING THE UNIT FOR AN EXTENDED PERIOD OF TIME, IT REMAINS ACTIVE FOR A BRIEF TIME (1-3 SECONDS) AFTER THE FOOTSWITCH IS RELEASED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 CROSSFIRE FOOTSWITCH FOOTSWITCH GEI STRYKER ENDOSCOPY SAN JOSE

    Patients

    Seq Age Sex Outcome Treatment
    1 UNK