BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    SECURE 3 MED/SURG BED

    MDR report key: 2931661 · Received January 28, 2013

    Report

    Report Number
    0001831750-2013-00444
    Event Type
    Malfunction
    Date Received
    January 28, 2013
    Date of Event
    January 7, 2013
    Report Date
    January 7, 2013
    Manufacturer
    STRYKER MEDICAL-KALAMAZOO
    Product Code
    FNL
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    WA, US
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 1

    RESULT: POWER SENSOR COIL CABLE. RESULT: GATCH LITTER COVER. CONCLUSION : SERVICE TECHNICIAN WILL RETURN AT A LATER DATE TO COMPLETE BED REPAIR.

    Description of Event or Problem · 1

    IT WAS REPORTED BY SERVICE REPORT THAT THE FOOTEND MOTOR WOULD SPARK WHEN THE BED WAS PLUGGED IN AND THE BED WAS STUCK AT AN ELEVATED HEIGHT.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    37647 SECURE 3 MED/SURG BED BED, AC-POWERED ADJUSTABLE HOSPITAL FNL STRYKER MEDICAL-KALAMAZOO

    Patients

    Seq Age Sex Outcome Treatment
    1