BEUDAMED
    FDA Adverse Event Injury Summary report: N

    EZ-PRO R4 AMBUL COT OBS(5/08)

    MDR report key: 2981235 · Received February 27, 2013

    Report

    Report Number
    0001831750-2013-01564
    Event Type
    Injury
    Date Received
    February 27, 2013
    Date of Event
    February 11, 2013
    Report Date
    February 11, 2013
    Manufacturer
    STRYKER MEDICAL-KALAMAZOO
    Product Code
    FPO
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    MI, US
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 1

    AS A RESULT OF THE DROP THE PATIENT ALLEGED OF PAIN IN THE NECK AND SPINE.

    Description of Event or Problem · 1

    IT WAS REPORTED TO THE FIELD SERVICE TECHNICIAN FOR STRYKER THAT WHILE TRANSPORTING A PATIENT THE COT WENT FROM INTERMEDIATE POSITION TO FULL POSITION . FURTHER INVESTIGATION FROM THE STRYKER FIELD SERVICE TECHNICIAN REVEALED THAT THE COT WAS IN BAD SHAPE AND THE CUSTOMER WILL BE REMOVING THE UNIT FROM SERVICE. THE PATIENT WAS ALLEGEDLY EXPERIENCING PAIN BUT COMPLAINANT IS NOT AWARE OF MEDICAL INTERVENTION.

    Description of Event or Problem · 1

    IT WAS REPORTED TO THE FIELD SERVICE TECHNICIAN FOR STRYKER THAT WHILE TRANSPORTING A PATIENT THE COT WENT FROM INTERMEDIATE POSITION TO FULL POSITION. FURTHER INVESTIGATION FROM THE STRYKER FIELD SERVICE TECHNICIAN REVEALED THAT THE COT WAS IN BAD SHAPE AND THE CUSTOMER WILL BE REMOVING THE UNIT FROM SERVICE. THE PATIENT WAS ALLEGEDLY EXPERIENCING PAIN BUT COMPLAINANT IS NOT AWARE OF MEDICAL INTERVENTION.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    84389 EZ-PRO R4 AMBUL COT OBS(5/08) STRETCHER, WHEELED FPO STRYKER MEDICAL-KALAMAZOO

    Patients

    Seq Age Sex Outcome Treatment
    1