BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    RENAISSANCE 29 STRETCHER

    MDR report key: 2961472 · Received January 17, 2013

    Report

    Report Number
    1831750-2013-90505
    Event Type
    Malfunction
    Date Received
    January 17, 2013
    Date of Event
    November 28, 2012
    Report Date
    November 28, 2012
    Manufacturer
    STRYKER MEDICAL
    Product Code
    FPO
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    VA, US
    Reporter Occupation
    UNKNOWN

    Narratives

    Additional Manufacturer Narrative · 1

    THE REASON FOR THE SERIALIZATION STARTING WITH 90XXX IS TO PROVIDE CLARIFICATION FOLLOWING A CHANGE IN STRYKER'S ELECTRONIC COMPLAINT SYSTEMS.

    Description of Event or Problem · 1

    IT WAS REPORTED BY SERVICE REPORT THAT THE FOOT END JACK COULD NOT BE FULLY RAISED. NO PT INVOLVEMENT OR ADVERSE CONSEQUENCES ARE REPORTED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    26965 RENAISSANCE 29 STRETCHER HOSPITAL WHEELED STRETCHER FPO STRYKER MEDICAL 1711 NA

    Patients

    Seq Age Sex Outcome Treatment
    1