BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    GOBED II

    MDR report key: 2031766 · Received February 25, 2011

    Report

    Report Number
    1831750-2011-01890
    Event Type
    Malfunction
    Date Received
    February 25, 2011
    Date of Event
    January 24, 2011
    Report Date
    January 26, 2011
    Manufacturer
    STRYKER MEDICAL
    Product Code
    FNL
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    MD, US
    Reporter Occupation
    UNKNOWN

    Narratives

    Description of Event or Problem · 1

    IT WAS REPORTED THAT BED EXPERIENCED FLUID ENTERING THE MOTOR CONTROL BOARD, CAUSING A SHORT CIRCUIT. NO PATIENT INVOLVEMENT OR ADVERSE EVENT REPORTED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 GOBED II A/C HOPSITAL BED FNL STRYKER MEDICAL FL28EX NA

    Patients

    Seq Age Sex Outcome Treatment
    1 UNK