BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    ELECTRIC MED/SURG BED

    MDR report key: 2112551 · Received May 25, 2011

    Report

    Report Number
    1831750-2011-05050
    Event Type
    Malfunction
    Date Received
    May 25, 2011
    Date of Event
    April 27, 2011
    Report Date
    April 27, 2011
    Manufacturer
    FLEXTRONICS EMS CANADA
    Product Code
    FNL
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    WI, US
    Reporter Occupation
    UNKNOWN

    Narratives

    Additional Manufacturer Narrative · 1

    POWER CORD NOT PROPERLY SECURED TO BED.

    Description of Event or Problem · 1

    IT WAS REPORTED BY SERVICE REPORT THAT THE BED HAS NO POWER. THERE WAS PT INVOLVEMENT; HOWEVER NO ADVERSE CONSEQUENCES ARE REPORTED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 ELECTRIC MED/SURG BED A/C HOSPITAL BED FNL FLEXTRONICS EMS CANADA FL23SE NA

    Patients

    Seq Age Sex Outcome Treatment
    1 UNK