BEUDAMED
    FDA Adverse Event Other Summary report: N

    MX-PRO AMBULANCE COT OBS 10/01

    MDR report key: 2132744 · Received June 10, 2011

    Report

    Report Number
    1831750-2011-05818
    Event Type
    Other
    Date Received
    June 10, 2011
    Date of Event
    May 16, 2011
    Report Date
    May 16, 2011
    Manufacturer
    STRYKER MEDICAL
    Product Code
    INK
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    CA, US
    Reporter Occupation
    UNKNOWN

    Narratives

    Additional Manufacturer Narrative · 1

    UPON INVESTIGATION, IT WAS FOUND THAT THE OPERATORS WERE NOT USING THE COT PROPERLY. CONCLUSION: THE ISSUE WAS RESOLVED FOR THE CUSTOMER BY TRAINING THE STAFF MEMBERS THAT DID NOT KNOW HOW TO PROPERLY OPERATE THE COT. ADDITIONALLY, INFO ON THE USE AND MAINTENANCE OF THE COT WAS SENT TO THE STAFF MEMBERS FROM THE SERVICE TECH.

    Description of Event or Problem · 1

    IT WAS REPORTED BY SERVICE REPORT THAT THE SECURITY STAFF STATED THAT THE COT LEGS STICK WHEN RAISING OR LOWERING. THERE WAS PT INVOLVEMENT; HOWEVER, NO ADVERSE CONSEQUENCES WERE REPORTED.

    Devices

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

    Patients

    Seq Age Sex Outcome Treatment
    1