BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    EZ-PRO AMBULANCE COT OBS 11/99

    MDR report key: 2981234 · Received February 27, 2013

    Report

    Report Number
    0001831750-2013-01561
    Event Type
    Malfunction
    Date Received
    February 27, 2013
    Date of Event
    February 5, 2013
    Report Date
    February 5, 2013
    Manufacturer
    STRYKER MEDICAL-KALAMAZOO
    Product Code
    FPO
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    TX, US
    Reporter Occupation
    OTHER

    Narratives

    Description of Event or Problem · 1

    IT WAS REPORTED VIA REPAIR WORK ORDER THAT THE LOCKING PIN ON THE PATIENT-LEFT SIDE WOULD NOT ENGAGE AND LOCK IN PROPERLY. FURTHERMORE, NO ADVERSE CONSEQUENCE OR CLINICALLY RELEVANT DELAY IN TREATMENT WAS REPORTED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    83879 EZ-PRO AMBULANCE COT OBS 11/99 STRETCHER, WHEELED FPO STRYKER MEDICAL-KALAMAZOO

    Patients

    Seq Age Sex Outcome Treatment
    1