BEUDAMED
    FDA Adverse Event Other Summary report: N

    STRYKER ENDOSCOPY

    MDR report key: 826883 · Received March 8, 2007

    Report

    Report Number
    MW1042166
    Event Type
    Other
    Date Received
    March 8, 2007
    Date of Event
    October 31, 2006
    Manufacturer
    STRYKER ENDOSCOPY
    Product Code
    HRX
    Product Problem
    Yes
    Report Source
    Voluntary report
    Reporter Location
    CA, US
    Reporter Occupation
    RISK MANAGER

    Narratives

    Description of Event or Problem · 1

    MFR DEFECT: WATER LEAKAGE.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 STRYKER ENDOSCOPY TUBING SET FOR ARTHROSCOPY PUMP HRX STRYKER ENDOSCOPY 97-1099-95 H SL06272

    Patients

    Seq Age Sex Outcome Treatment
    1 58 YR Other