BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    GO BED PLUS

    MDR report key: 3142832 · Received June 3, 2013

    Report

    Report Number
    0001831750-2013-05016
    Event Type
    Malfunction
    Date Received
    June 3, 2013
    Date of Event
    May 10, 2013
    Report Date
    May 10, 2013
    Manufacturer
    STRYKER MEDICAL-KALAMAZOO
    Product Code
    FNL
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    NY, US
    Reporter Occupation
    OTHER

    Narratives

    Description of Event or Problem · 1

    IT WAS REPORTED VIA REPAIR WORK ORDER THAT THE FOOT LEFT SIDERAIL WAS STUCK IN THE LOWEST POSITION DUE TO TIMING LINK CORROSION CAUSED BY FLUID INTRUSION. IT WAS ALSO REPORTED THAT THE POWER CORD GROUND PRONG WAS MISSING. NO PATIENT WAS AFFECTED AND NO ADVERSE CONSEQUENCE OR CLINICALLY RELEVANT DELAY IN TREATMENT WAS REPORTED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    245242 GO BED PLUS BED, AC-POWERED ADJUSTABLE HOSPITAL FNL STRYKER MEDICAL-KALAMAZOO

    Patients

    Seq Age Sex Outcome Treatment
    1