BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    STRETCHER

    MDR report key: 1900952 · Received November 10, 2010

    Report

    Report Number
    1831750-2010-03660
    Event Type
    Malfunction
    Date Received
    November 10, 2010
    Date of Event
    October 14, 2010
    Report Date
    October 14, 2010
    Manufacturer
    STRYKER CORP., MEDICAL DIVISION
    Product Code
    FPO
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    NY, US
    Reporter Occupation
    UNKNOWN

    Narratives

    Description of Event or Problem · 1

    IT WAS REPORTED BY SERVICE REPORT THAT THE HEAD END JACK WILL NOT RAISE AND IS LEAKING HYDRAULIC FLUID. THE BRAKES ARE OUT OF ADJUSTMENT AND THE SIDE RAILS LOOSE AND WILL NOT LATCH. NO PT INVOLVEMENT OR ADVERSE CONSEQUENCES ARE REPORTED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 STRETCHER HOSPITAL WHEELED STRETCHER FPO STRYKER CORP., MEDICAL DIVISION 1010 NA

    Patients

    Seq Age Sex Outcome Treatment
    1 NA