BEUDAMED
    FDA Adverse Event Injury Summary report: N

    POWER PRO IT AMBULANCE - OBS

    MDR report key: 3851157 · Received June 5, 2014

    Report

    Report Number
    0001831750-2014-03039
    Event Type
    Injury
    Date Received
    June 5, 2014
    Date of Event
    May 13, 2014
    Report Date
    May 13, 2014
    Manufacturer
    STRYKER MEDICAL-KALAMAZOO
    Product Code
    FPO
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    CA, US
    Reporter Occupation
    OTHER

    Narratives

    Description of Event or Problem · 1

    IT WAS REPORTED THAT THE SAFETY BAR MISSED THE SAFETY HOOK AND THE COT TIPPED. THE CUSTOMER REPORTED THAT THE COT TIPPED OVER AND FELL WITH AN INFANT WHILE THE AMBULANCE CREW WAS REMOVING THE COT FROM THE AMBULANCE. THE CUSTOMER REPORTED THAT THE INFANT WAS INJURED IN THE FALL. THE CUSTOMER REPORTED THAT THEY BELIEVE THAT THE AMBULANCE CREW REMOVED THE COT INCORRECTLY AND MISSED THE SAFETY HOOK. THE UNIT WAS EVALUATED BY A SERVICE TECHNICIAN WITH NO FAILURE DETECTED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    329932 POWER PRO IT AMBULANCE - OBS STRETCHER, WHEELED FPO STRYKER MEDICAL-KALAMAZOO

    Patients

    Seq Age Sex Outcome Treatment
    1