BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    EPIC II CRITICAL CARE BED

    MDR report key: 1915228 · Received November 16, 2010

    Report

    Report Number
    1831750-2010-03885
    Event Type
    Malfunction
    Date Received
    November 16, 2010
    Date of Event
    October 20, 2010
    Report Date
    October 20, 2010
    Manufacturer
    STRYKER CORP., MEDICAL DIV.
    Product Code
    FNL
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    ME, US
    Reporter Occupation
    OTHER

    Narratives

    Description of Event or Problem · 1

    IT WAS REPORTED BY SERVICE REPORT THAT THE UP/DOWN CONTROL BUTTONS ON FOOT BOARD AND SIDERAILS WERE INTERMITTENTLY NOT RESPONDING. NO PT INVOLVEMENT OR ADVERSE CONSEQUENCES ARE REPORTED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 EPIC II CRITICAL CARE BED A/C POWERED HOSPITAL BED FNL STRYKER CORP., MEDICAL DIV. 2030 EPIC NA

    Patients

    Seq Age Sex Outcome Treatment
    1