BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    SM304 M-SERIES W/ZOOM

    MDR report key: 1811482 · Received August 17, 2010

    Report

    Report Number
    1831750-2010-01848
    Event Type
    Malfunction
    Date Received
    August 17, 2010
    Date of Event
    July 24, 2010
    Report Date
    July 24, 2010
    Manufacturer
    STRYKER CORP, MEDICAL DIV.
    Product Code
    INK
    PMA / PMN Number
    K022309
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    KY, US
    Reporter Occupation
    UNKNOWN

    Narratives

    Description of Event or Problem · 1

    IT WAS REPORTED IN A SERVICE REPORT THAT THE FOOT END OF THE STRETCHER DIDN'T RAISE AND THE JACK WAS LEAKING FLUID ONTO THE FLOOR. NO ADVERSE CONSEQUENCES WERE ALLEGED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 SM304 M-SERIES W/ZOOM WHEELED POWERED STRETCHER INK STRYKER CORP, MEDICAL DIV. 1025 NA

    Patients

    Seq Age Sex Outcome Treatment
    1 NA