BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    TRIO MOBILE SURGY PLTFRM

    MDR report key: 2113468 · Received May 25, 2011

    Report

    Report Number
    1831750-2011-05078
    Event Type
    Malfunction
    Date Received
    May 25, 2011
    Date of Event
    April 27, 2011
    Report Date
    April 27, 2011
    Manufacturer
    STRYKER MEDICAL
    Product Code
    FPO
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    ID, US
    Reporter Occupation
    UNKNOWN

    Narratives

    Additional Manufacturer Narrative · 1

    EVALUATION RESULT: JACK LINKAGE, GUIDE INSERT.

    Description of Event or Problem · 1

    IT WAS REPORTED BY SERVICE REPORT THAT THE STRETCHER WOULD NOT RAISE OR LOWER WHEN ENGAGING THE PUMP PEDALS. THE GUIDE INSERT FOR THE FOOT SECTION OF THIS STRETCHER WAS BROKEN. NO PATIENT INVOLVEMENT OR ADVERSE CONSEQUENCES ARE REPORTED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 TRIO MOBILE SURGY PLTFRM HOSPITAL WHEELED STRETCHER FPO STRYKER MEDICAL 1033 NA

    Patients

    Seq Age Sex Outcome Treatment
    1