BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    MX-PRO AMBULANCE COT OBS 10/01

    MDR report key: 1811455 · Received August 17, 2010

    Report

    Report Number
    1831750-2010-01853
    Event Type
    Malfunction
    Date Received
    August 17, 2010
    Date of Event
    July 29, 2010
    Report Date
    July 29, 2010
    Manufacturer
    STRYKER CORP, MEDICAL DIV
    Product Code
    FPO
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    TX, US
    Reporter Occupation
    UNKNOWN

    Narratives

    Additional Manufacturer Narrative · 1

    LEAK.

    Description of Event or Problem · 1

    IT HAS BEEN REPORTED IN A SERVICE REPORT THAT THE FOWLER CYLINDER IS NOT HOLDING UP THE FOWLER. IT WAS FURTHER REPORTED THAT THE CYLINDER WAS LEAKING. NO ADVERSE CONSEQUENCES WERE ALLEGED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 MX-PRO AMBULANCE COT OBS 10/01 STRETCHER WHEELED FPO STRYKER CORP, MEDICAL DIV 6080 NA

    Patients

    Seq Age Sex Outcome Treatment
    1 UNK