BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    MX-PRO AMBULANCE COT

    MDR report key: 2143594 · Received June 2, 2011

    Report

    Report Number
    1831750-2011-05431
    Event Type
    Malfunction
    Date Received
    June 2, 2011
    Date of Event
    May 5, 2011
    Report Date
    May 5, 2011
    Manufacturer
    STRYKER MEDICAL
    Product Code
    FPO
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    TX, US
    Reporter Occupation
    UNKNOWN

    Narratives

    Additional Manufacturer Narrative · 1

    TRIGGER LOCK.

    Description of Event or Problem · 1

    IT WAS REPORTED BY THE SERVICE REPORT THAT THE BREAK AWAY HEAD SECTION WOULD NOT LOCK INTO PLACE DUE TO A BROKEN TRIGGER LOCK. NO PT INVOLVEMENT OR ADVERSE CONSEQUENCES ARE REPORTED.

    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