BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    GOBED II MED/SURG BED

    MDR report key: 2110427 · Received April 25, 2011

    Report

    Report Number
    1831750-2011-03946
    Event Type
    Malfunction
    Date Received
    April 25, 2011
    Date of Event
    March 28, 2011
    Report Date
    March 28, 2011
    Manufacturer
    STRYKER MEDICAL KALAMAZOO
    Product Code
    FNL
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    CT, US
    Reporter Occupation
    UNKNOWN

    Narratives

    Additional Manufacturer Narrative · 1

    LOOSE INTERNAL CONNECTIONS ON POWER PLUG.

    Description of Event or Problem · 1

    IT WAS REPORTED BY SERVICE REPORT THAT THE BED ALARM IS NOT WORKING AND INTERMITTENT POWER TO THE BED. IT IS UNK IF THERE WAS PT INVOLVEMENT, HOWEVER, NO ADVERSE CONSEQUENCES ARE REPORTED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 GOBED II MED/SURG BED IMPLANT FNL STRYKER MEDICAL KALAMAZOO FL28C NA

    Patients

    Seq Age Sex Outcome Treatment
    1 UNK