BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    GOBED II MED/SURG BED

    MDR report key: 2191602 · Received July 1, 2011

    Report

    Report Number
    1831750-2011-06681
    Event Type
    Malfunction
    Date Received
    July 1, 2011
    Date of Event
    June 3, 2011
    Report Date
    June 3, 2011
    Manufacturer
    FLEXTRONICS EMS CANADA
    Product Code
    FNL
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    MI, US
    Reporter Occupation
    UNKNOWN

    Narratives

    Additional Manufacturer Narrative · 1

    FAULTY HI-LO MOTOR.

    Description of Event or Problem · 1

    IT WAS REPORTED BY SERVICE REPORT THAT THE FOOT END HI-LO MOTOR WOULD NOT MOVE AND IT WAS STUCK IN THE UP POSITION. NO PT INVOLVEMENT OR ADVERSE CONSEQUENCES ARE REPORTED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 GOBED II MED/SURG BED A/C HOSPITAL BED FNL FLEXTRONICS EMS CANADA FL28E NA

    Patients

    Seq Age Sex Outcome Treatment
    1 UNK