BEUDAMED
    FDA Adverse Event Injury Summary report: N

    POWER PRO AMBULANCE COT - OBS

    MDR report key: 7616461 · Received June 19, 2018

    Report

    Report Number
    0001831750-2018-00601
    Event Type
    Injury
    Date Received
    June 19, 2018
    Date of Event
    May 19, 2018
    Report Date
    June 21, 2018
    Manufacturer
    STRYKER MEDICAL-KALAMAZOO
    Product Code
    FPO
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    SC, US
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 1

    IT WAS REPORTED MINOR INJURIES WERE SUSTAINED, WITHOUT SPECIFICATION OF WHAT THOSE INJURIES WERE OR WHO SUSTAINED THEM. THERE WAS NO REPORT OF ADVERSE CONSEQUENCES. THERE WAS NO ALLEGED MALFUNCTION OF THE STRYKER DEVICES ON THE AMBULANCE AT THE TIME OF THE ACCIDENT.

    Description of Event or Problem · 1

    IT WAS REPORTED THE USER FACILITY EXPERIENCED AN AMBULANCE ACCIDENT, IN WHICH A PATIENT WAS BEING TRANSPORTED. AS A RESULT OF THE ACCIDENT, BOTH PARAMEDICS WERE TRANSPORTED TO THE HOSPITAL. IT IS CURRENTLY UNKNOWN IF ANY INJURIES WERE SUSTAINED BY THE PARAMEDICS OR PATIENT, OR WHETHER MEDICAL INTERVENTION WAS NECESSARY.

    Description of Event or Problem · 1

    IT WAS REPORTED THE USER FACILITY EXPERIENCED AN AMBULANCE ACCIDENT, IN WHICH A PATIENT WAS BEING TRANSPORTED. AS A RESULT OF THE ACCIDENT, BOTH PARAMEDICS WERE TRANSPORTED TO THE HOSPITAL. IT WAS REPORTED MINOR INJURIES WERE SUSTAINED, WITHOUT SPECIFICATION OF WHAT THOSE INJURIES WERE OR WHO SUSTAINED THEM. THERE WAS NO REPORT OF ADVERSE CONSEQUENCES. THERE WAS NO ALLEGED MALFUNCTION OF THE STRYKER DEVICES ON THE AMBULANCE AT THE TIME OF THE ACCIDENT.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    457882 POWER PRO AMBULANCE COT - OBS STRETCHER, WHEELED FPO STRYKER MEDICAL-KALAMAZOO

    Patients

    Seq Age Sex Outcome Treatment
    1