BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    GOBED II MED/SURG BED

    MDR report key: 1827890 · Received September 2, 2010

    Report

    Report Number
    9680128-2010-00106
    Event Type
    Malfunction
    Date Received
    September 2, 2010
    Date of Event
    April 1, 2010
    Report Date
    April 12, 2010
    Manufacturer
    STRYKER MEDICAL QUEBEC LP
    Product Code
    FNL
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    CI
    Reporter Occupation
    OTHER

    Narratives

    Description of Event or Problem · 1

    IT WAS REPORTED THAT BEDS PRESENT AUTOMATIC ACTIVATION OF THE ENGINE OF FEET, WITHOUT PRESSING THE COMMANDS OF THE SIDE RAILS, THE PROBLEM IS GENERATED BY CONDUCTIVITY IN THE CONNECTOR LEFT RAIL OF PT. NO INJURY REPORTED. "WE DID MEASURE BETWEEN PIN 8 AND 7 (THIGH UP), THEY PRESENT CONTINUITY IN EVERY MOMENT. WE REMOVED THE SILICON PRESENT ON THE CONNECTOR AND THE PROBLEMS FIXED." IF YOU WANT MORE INFO, WE HAVE PICTURES AND VIDEOS WITH THE PROBLEM.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 GOBED II MED/SURG BED HOSPITAL BED, A-C POWERED, ADJUSTABLE FNL STRYKER MEDICAL QUEBEC LP FL28C NA

    Patients

    Seq Age Sex Outcome Treatment
    1 UNK