BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    GOBED+

    MDR report key: 2072684 · Received April 21, 2011

    Report

    Report Number
    1831750-2011-03865
    Event Type
    Malfunction
    Date Received
    April 21, 2011
    Date of Event
    September 14, 2010
    Report Date
    September 14, 2010
    Manufacturer
    STRYKER MEDICAL
    Product Code
    FNL
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    AR, US
    Reporter Occupation
    UNKNOWN

    Narratives

    Additional Manufacturer Narrative · 1

    RESULT: FAULTY FOOT-END LOAD CELLS.

    Description of Event or Problem · 1

    IT WAS REPORTED IN A SERVICE REPORT THAT THE SCALE WAS NOT WORKING PROPERLY. NO PATIENT INVOLVEMENT OR ADVERSE CONSEQUENCES WERE REPORTED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 GOBED+ A/C POWERED HOSPITAL BED FNL STRYKER MEDICAL FL20E NA

    Patients

    Seq Age Sex Outcome Treatment
    1