BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    EPIC II CRITICAL CARE BED

    MDR report key: 2940643 · Received December 12, 2012

    Report

    Report Number
    1831750-2012-12835
    Event Type
    Malfunction
    Date Received
    December 12, 2012
    Date of Event
    December 1, 2012
    Report Date
    December 1, 2012
    Manufacturer
    STRYKER MEDICAL
    Product Code
    FNL
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    AL, US
    Reporter Occupation
    UNKNOWN

    Narratives

    Description of Event or Problem · 1

    IT WAS REPORTED BY SERVICE REPORT THAT THE POWER CORD HAD BROKEN GROUND PRONG. CUSTOMER REPORTED NO PT INVOLVEMENT OR ADVERSE CONSEQUENCES REPORTED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 EPIC II CRITICAL CARE BED AC POWERED HOSPITAL BED FNL STRYKER MEDICAL 2030 NA

    Patients

    Seq Age Sex Outcome Treatment
    1