BEUDAMED
    FDA Adverse Event Other Summary report: N

    GOBED II

    MDR report key: 1873940 · Received September 30, 2010

    Report

    Report Number
    9680128-2010-00136
    Event Type
    Other
    Date Received
    September 30, 2010
    Date of Event
    September 22, 2010
    Report Date
    September 22, 2010
    Manufacturer
    STRYKER MEDICAL QUEBEC LP
    Product Code
    FNL
    Report Source
    Manufacturer report
    Reporter Location
    FL, US
    Reporter Occupation
    OTHER

    Narratives

    Description of Event or Problem · 1

    IT WAS REPORTED THAT THE FACILITY HAD TWO REPORTED INCIDENTS OF ARCHING AT THE HEADWALL OF THE BED WHERE THE POWER CORD PLUGS INTO THE BED. NO ADVERSE CONSEQUENCE WAS SEEN IN EITHER CASE. NO INJURY REPORTED.

    Devices

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

    Patients

    Seq Age Sex Outcome Treatment
    1 UNK