BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    TRANSPORT SERIES

    MDR report key: 2915112 · Received December 7, 2012

    Report

    Report Number
    1831750-2012-12620
    Event Type
    Malfunction
    Date Received
    December 7, 2012
    Date of Event
    September 10, 2012
    Report Date
    December 4, 2012
    Manufacturer
    STRYKER MEDICAL
    Product Code
    FPO
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    FR
    Reporter Occupation
    UNKNOWN

    Narratives

    Description of Event or Problem · 1

    ON (B)(4) 2012: INITIAL MDR BEING ISSUED. ADDITIONAL NEW INFO WAS RECEIVED 12/04/2012: JACK COULD NOT BE LOWERED OR RAISED TO FULL EXTENT.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 TRANSPORT SERIES HOSPITAL WHEELED STRETCHER FPO STRYKER MEDICAL 0721 NA

    Patients

    Seq Age Sex Outcome Treatment
    1