BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    RENAISSANCE 29

    MDR report key: 2213005 · Received July 12, 2011

    Report

    Report Number
    1831750-2011-06904
    Event Type
    Malfunction
    Date Received
    July 12, 2011
    Date of Event
    June 13, 2011
    Report Date
    June 13, 2011
    Manufacturer
    STRYKER MEDICAL
    Product Code
    FPO
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    TN, US
    Reporter Occupation
    UNKNOWN

    Narratives

    Description of Event or Problem · 1

    IT WAS REPORTED BY SVC REPORT THAT THE STRETCHER'S FOOT END JACK COULD NOT BE PUMPED UP. NO PT INVOLVEMENT OR ADVERSE CONSEQUENCES ARE REPORTED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 RENAISSANCE 29 HOSPITAL WHEELED STRETCHER FPO STRYKER MEDICAL 1711 NA

    Patients

    Seq Age Sex Outcome Treatment
    1