BEUDAMED
    FDA Adverse Event Other Summary report: N

    KARL STORZ RESECTOSCOPE

    MDR report key: 92406 · Received May 14, 1997

    Report

    Report Number
    2020550-1997-00017
    Event Type
    Other
    Date Received
    May 14, 1997
    Date of Event
    March 31, 1997
    Report Date
    May 12, 1997
    Manufacturer
    KARL STORZ ENDOSCOPY-AMERICA, INC.
    Product Code
    FED
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    CO, US
    Reporter Occupation
    OTHER

    Narratives

    Description of Event or Problem · 1

    DURING A TURP PROCEDURE WHILE PT WAS ON THE TABLE, THE LOOP WOULD NOT LOCK INTO THE RESECTOSCOPE. PROCEDURE CANCELED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 KARL STORZ RESECTOSCOPE RESECTOSCOPE FED KARL STORZ ENDOSCOPY-AMERICA, INC. 27050E *

    Patients

    Seq Age Sex Outcome Treatment
    1 55 YR Other