BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    ELECTRIC STRETCHER 12/09

    MDR report key: 2942492 · Received February 4, 2013

    Report

    Report Number
    0001831750-2013-00689
    Event Type
    Malfunction
    Date Received
    February 4, 2013
    Date of Event
    January 10, 2013
    Report Date
    January 10, 2013
    Manufacturer
    STRYKER MEDICAL-KALAMAZOO
    Product Code
    FPO
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    NC, US
    Reporter Occupation
    OTHER

    Narratives

    Description of Event or Problem · 1

    IT WAS REPORTED BY SERVICE REPORT THAT THE FOOT END JACK COULD NOT BE RAISED OR LOWERED FULLY.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    46992 ELECTRIC STRETCHER 12/09 STRETCHER, WHEELED FPO STRYKER MEDICAL-KALAMAZOO 1550

    Patients

    Seq Age Sex Outcome Treatment
    1