BEUDAMED
    FDA Adverse Event Other Summary report: N

    KARL STORZ

    MDR report key: 2903249 · Received December 28, 2012

    Report

    Report Number
    9610617-2012-00047
    Event Type
    Other
    Date Received
    December 28, 2012
    Date of Event
    February 1, 2012
    Report Date
    December 27, 2012
    Manufacturer
    KARL STORZ GMBH & CO. KG
    Product Code
    FEO
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    TX, US
    Reporter Occupation
    OTHER HEALTH CARE PROFESSIONAL

    Narratives

    Description of Event or Problem · 1

    ALLEGEDLY, PATIENT WAS UNDER ANESTHESIA AND PREPPED FOR A PROCEDURE, SCOPE WAS SET-UP FOR USE AND THERE WAS NO IMAGE. THE HOSPITAL DID NOT HAVE A BACKUP SCOPE AVAILABLE. PROCEDURE HAD TO BE ABORTED WITHOUT COMPLETION.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 KARL STORZ NEPHROSCOPE FEO KARL STORZ GMBH & CO. KG UNKNOWN NA

    Patients

    Seq Age Sex Outcome Treatment
    1 66 YR Other