BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    GO BED PLUS

    MDR report key: 2110434 · Received April 25, 2011

    Report

    Report Number
    1831750-2011-03949
    Event Type
    Malfunction
    Date Received
    April 25, 2011
    Date of Event
    March 29, 2011
    Report Date
    March 29, 2011
    Manufacturer
    STRYKER MEDICAL
    Product Code
    FNL
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    NY, US
    Reporter Occupation
    UNKNOWN

    Narratives

    Additional Manufacturer Narrative · 1

    RESULTS: THE SIDE RAILS WERE REMOVED FROM THE UNIT BY THE FACILITY.

    Description of Event or Problem · 1

    IT WAS REPORTED BY SERVICE REPORT THAT THE BED HAD INTERMITTENT POWER, A MISSING GROUND PRONG, AND ALL THE RAILS HAVE BEEN TAKEN OFF TO PUT ON OTHER BEDS. NO PATIENT INVOLVEMENT OR ADVERSE CONSEQUENCES ARE REPORTED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 GO BED PLUS A/C HOSPITAL BED FNL STRYKER MEDICAL 2501 NA

    Patients

    Seq Age Sex Outcome Treatment
    1 UNK