BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    FLUOROSCOPY STRETCHER

    MDR report key: 2920424 · Received December 7, 2012

    Report

    Report Number
    1831750-2012-12581
    Event Type
    Malfunction
    Date Received
    December 7, 2012
    Date of Event
    November 7, 2012
    Report Date
    November 7, 2012
    Manufacturer
    STRYKER MEDICAL
    Product Code
    FPO
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    TX, US
    Reporter Occupation
    UNKNOWN

    Narratives

    Description of Event or Problem · 1

    IT WAS REPORTED BY SVC REPORT THAT THE FOOT END JACK COULD NOT BE LOWERED DUE TO THE LOWERING RELEASE PEDAL EXTENSION SPRING BEING BROKEN, CAUSING THE RELEASE PEDAL TO BE INOPERABLE. NO PT INVOLVEMENT OR ADVERSE CONSEQUENCES ARE REPORTED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 FLUOROSCOPY STRETCHER HOSPITAL WHEELED STRETCHER FPO STRYKER MEDICAL 1080 NA

    Patients

    Seq Age Sex Outcome Treatment
    1