BEUDAMED
    FDA Adverse Event Injury Summary report: N

    RVSCH

    MDR report key: 232594 · Received July 6, 1999

    Report

    Report Number
    232594
    Event Type
    Injury
    Date Received
    July 6, 1999
    Date of Event
    September 20, 1998
    Report Date
    July 6, 1999
    Manufacturer
    RUSCH INC.
    Product Code
    FEI
    Report Source
    User Facility report
    Reporter Location
    PA, US
    Reporter Occupation
    RISK MANAGER

    Narratives

    Description of Event or Problem · 1

    CANTOR TUBE INSERTED MERCURY INSTILLED. X-RAY REVEALED MERCURY IN STOMACH 10/7/98 MFR SENT MORE THOROUGH INSTRUCTIONS FOR INSERTION.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 RVSCH CANTOR TUBE FEI RUSCH INC. * *

    Patients

    Seq Age Sex Outcome Treatment
    1 80 YR Hospitalization| R