BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    MX-PRO AMBULANCE COT OBS 10/01

    MDR report key: 3150395 · Received June 6, 2013

    Report

    Report Number
    0001831750-2013-05139
    Event Type
    Malfunction
    Date Received
    June 6, 2013
    Date of Event
    May 10, 2013
    Report Date
    May 10, 2013
    Manufacturer
    STRYKER MEDICAL-KALAMAZOO
    Product Code
    FPO
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    AL, US
    Reporter Occupation
    OTHER

    Narratives

    Description of Event or Problem · 1

    IT WAS REPORTED VIA REPAIR WORK ORDER THAT THE COT WAS MISSING THE SHOULDER HARNESS WHICH WOULD NOT ALLOW FOR PROPER SECURING OF A PATIENT. 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
    249886 MX-PRO AMBULANCE COT OBS 10/01 STRETCHER, WHEELED FPO STRYKER MEDICAL-KALAMAZOO

    Patients

    Seq Age Sex Outcome Treatment
    1