BEUDAMED
    FDA Adverse Event Injury Summary report: N

    SKYTRON

    MDR report key: 499485 · Received December 3, 2003

    Report

    Report Number
    499485
    Event Type
    Injury
    Date Received
    December 3, 2003
    Date of Event
    October 15, 2003
    Manufacturer
    SKYTRON
    Product Code
    FWY
    Report Source
    User Facility report
    Reporter Location
    AZ, US
    Reporter Occupation
    INVALID DATA

    Narratives

    Description of Event or Problem · 1

    PATIENT WAS IN OR SUITE FOR COLECTOMY. THE OR TABLE WAS BEING RAISED INTO THE LITHOTOMY POSITION WHEN THE NURSE NOTICED THE ELECTRICAL CORD WAS ON FIRE.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 SKYTRON OR BED (HYDRAULIC) EE21917 FWY SKYTRON 21917 *

    Patients

    Seq Age Sex Outcome Treatment
    1 82 YR Required Intervention