BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    GOBED II MED/SURG BED

    MDR report key: 2933420 · Received December 21, 2012

    Report

    Report Number
    1831750-2012-13063
    Event Type
    Malfunction
    Date Received
    December 21, 2012
    Date of Event
    November 26, 2012
    Report Date
    November 27, 2012
    Manufacturer
    FLEXTRONIC EMS CANADA
    Product Code
    FNL
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    SA
    Reporter Occupation
    UNKNOWN

    Narratives

    Additional Manufacturer Narrative · 1

    RESULT - CONTROL BOARD.

    Description of Event or Problem · 1

    IT WAS REPORTED THAT THE BED HAD STOPPED WORKING. THERE WAS NO PT INVOLVEMENT OR ADVERSE CONSEQUENCES REPORTED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 GOBED II MED/SURG BED A/C HOSPITAL BED FNL FLEXTRONIC EMS CANADA FL28C NA

    Patients

    Seq Age Sex Outcome Treatment
    1