BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    STRYKER CORPORATION

    MDR report key: 144675 · Received January 16, 1998

    Report

    Report Number
    MW1012819
    Event Type
    Malfunction
    Date Received
    January 16, 1998
    Date of Event
    January 7, 1998
    Report Date
    January 9, 1998
    Manufacturer
    STRYKER CORP.
    Product Code
    GEI
    Product Problem
    Yes
    Report Source
    Voluntary report
    Reporter Location
    FL, US
    Reporter Occupation
    NURSE

    Narratives

    Description of Event or Problem · 1

    BROKEN WIRES AT CONNECTION TO GENERATOR. THEN CABLE SPARKS. NO HARM TO THIS PT.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 STRYKER CORPORATION CORD GEI STRYKER CORP. * *

    Patients

    Seq Age Sex Outcome Treatment
    1 42 YR Other