BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    MX-PRO AMBULANCE COT

    MDR report key: 2031410 · Received February 24, 2011

    Report

    Report Number
    1831750-2011-01874
    Event Type
    Malfunction
    Date Received
    February 24, 2011
    Date of Event
    October 27, 2010
    Report Date
    October 27, 2010
    Manufacturer
    STRYKER MEDICAL
    Product Code
    FPO
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    GA, US
    Reporter Occupation
    UNKNOWN

    Narratives

    Description of Event or Problem · 1

    IT WAS REPORTED BY SVC REPORT THAT THE COT DID NOT MEET SPECIFICATION; THE TORSION SPRINGS, WHEELS, AND CLEVIS PINS NEEDED TO BE REPLACED. THERE WERE NO ADVERSE CONSEQUENCES.

    Devices

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

    Patients

    Seq Age Sex Outcome Treatment
    1