BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    EZ-PRO AMBULANCE COT OBS 11/99

    MDR report key: 3142073 · Received June 3, 2013

    Report

    Report Number
    0001831750-2013-05006
    Event Type
    Malfunction
    Date Received
    June 3, 2013
    Date of Event
    May 6, 2013
    Report Date
    May 6, 2013
    Manufacturer
    STRYKER MEDICAL-KALAMAZOO
    Product Code
    FPO
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    IN, US
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 1

    THE CUSTOMER NO LONGER NEEDED ASSISTANCE BY STRYKER AND RESOLVED THE ALLEGED ISSUE INTERNALLY.

    Description of Event or Problem · 1

    IT WAS REPORTED THAT THE COT COULD NOT BE LOADED INTO THE AMBULANCE. NO PATIENT WAS AFFECTED AND NO ADVERSE CONSEQUENCE OR CLINICALLY RELEVANT DELAY IN TREATMENT WAS REPORTED.

    Description of Event or Problem · 1

    IT WAS REPORTED THAT THE COT COULD NOT BE LOADED INTO THE AMBULANCE. NO PATIENT WAS AFFECTED AND NO ADVERSE CONSEQUENCE OR CLINICALLY RELEVANT DELAY IN TREATMENT WAS REPORTED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    244363 EZ-PRO AMBULANCE COT OBS 11/99 STRETCHER, WHEELED FPO STRYKER MEDICAL-KALAMAZOO

    Patients

    Seq Age Sex Outcome Treatment
    1