BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    MX-PRO R-3 AMBULANCE COT

    MDR report key: 1760137 · Received July 12, 2010

    Report

    Report Number
    1831750-2010-01493
    Event Type
    Malfunction
    Date Received
    July 12, 2010
    Date of Event
    June 15, 2010
    Report Date
    June 15, 2010
    Manufacturer
    STRYKER CORP, MEDICAL DIVISION
    Product Code
    FPO
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    CA, US
    Reporter Occupation
    OTHER

    Narratives

    Description of Event or Problem · 1

    IT WAS REPORTED IN A SERVICE REPORT THAT THE BREAKAWAY HEAD SECTION WAS DAMAGED. NO ADVERSE CONSEQUENCES ALLEGED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 MX-PRO R-3 AMBULANCE COT STRETCHER WHEELED FPO STRYKER CORP, MEDICAL DIVISION 6082 NA

    Patients

    Seq Age Sex Outcome Treatment
    1 UNK