BEUDAMED
    FDA Adverse Event Other Summary report: N

    STRYKER 596 CAMERA CCU

    MDR report key: 285742 · Received July 12, 2000

    Report

    Report Number
    2936485-2000-00070
    Event Type
    Other
    Date Received
    July 12, 2000
    Date of Event
    July 7, 2000
    Report Date
    July 10, 2000
    Manufacturer
    STRYKER ENDOSCOPY
    Product Code
    HRX
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    CA, US
    Reporter Occupation
    OTHER

    Narratives

    Description of Event or Problem · 1

    IT WAS ALLEGED THAT AFTER A PROCEDURE, THE NURSE WAS HANDED THE CAMERA AND RECEIVED AN ELECTRICAL SHOCK. IT WAS REPORTED THAT NURSE WAS NOT WEARING GLOVES.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 STRYKER 596 CAMERA CCU CAMERA CCU HRX STRYKER ENDOSCOPY 0596-010-000 NA

    Patients

    Seq Age Sex Outcome Treatment
    1 *