BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    GOBED II MED/SURG BED

    MDR report key: 2190664 · Received July 29, 2011

    Report

    Report Number
    1831750-2011-07886
    Event Type
    Malfunction
    Date Received
    July 29, 2011
    Date of Event
    July 1, 2011
    Report Date
    July 1, 2011
    Manufacturer
    STRYKER MEDICAL
    Product Code
    FNL
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    FL, US
    Reporter Occupation
    UNKNOWN

    Narratives

    Additional Manufacturer Narrative · 1

    RESULTS: LOOSE WIRE IN POWER CONNECTOR TO CONTROL BOARD.

    Description of Event or Problem · 1

    IT WAS REPORTED BY SERVICE REPORT THAT THERE WAS NO POWER TO THE BED FUNCTIONS. NO PATIENT INVOLVEMENT. NO PATIENT 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 STRYKER MEDICAL FL28C NA

    Patients

    Seq Age Sex Outcome Treatment
    1 UNK