BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    GOBED II

    MDR report key: 2820896 · Received October 4, 2012

    Report

    Report Number
    1831750-2012-10355
    Event Type
    Malfunction
    Date Received
    October 4, 2012
    Date of Event
    September 4, 2012
    Report Date
    September 4, 2012
    Manufacturer
    FLEXTRONICS EMS CANADA
    Product Code
    FNL
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    KS, US
    Reporter Occupation
    UNKNOWN

    Narratives

    Description of Event or Problem · 1

    IT WAS REPORTED BY SERVICE REPORT THAT THE FOOT END OF THE BED WILL NOT MOVE. NO PT INVOLVEMENT OR ADVERSE CONSEQUENCES ARE REPORTED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 GOBED II A/C HOSPITAL BED FNL FLEXTRONICS EMS CANADA FL28EX NA

    Patients

    Seq Age Sex Outcome Treatment
    1