BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    MX-PRO AMBULANCE COT

    MDR report key: 1894654 · Received November 5, 2010

    Report

    Report Number
    1831750-2010-03529
    Event Type
    Malfunction
    Date Received
    November 5, 2010
    Date of Event
    July 30, 2010
    Report Date
    July 30, 2010
    Manufacturer
    STRYKER CORP., MEDICAL DIVISION
    Product Code
    FPO
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    NV, US
    Reporter Occupation
    UNKNOWN

    Narratives

    Description of Event or Problem · 1

    IT WAS REPORTED IN A SERVICE REPORT THE LEGS WERE NOT RETRACTING PROPERLY. NO ADVERSE CONSEQUENCES OR INJURIES WERE REPORTED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 MX-PRO AMBULANCE COT STRETCHER, WHEELED FPO STRYKER CORP., MEDICAL DIVISION 6080 NA

    Patients

    Seq Age Sex Outcome Treatment
    1