BEUDAMED
    FDA Adverse Event Other Summary report: N

    FERNO PROFLEXX 35X AMBULANCE STRETCHER

    MDR report key: 1235705 · Received November 17, 2008

    Report

    Report Number
    1523574-2008-00015
    Event Type
    Other
    Date Received
    November 17, 2008
    Date of Event
    August 28, 2008
    Report Date
    November 17, 2008
    Manufacturer
    FERNO-WASHINGTON, INC.
    Product Code
    FPO
    Report Source
    Manufacturer report
    Reporter Location
    IL, US
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 1

    MANUFACTURER HAS PROVIDED END USER WITH A LOANER AND REQUESTED RETURN OF INCIDENT STRETCHER. STRETCHER NOT YET RECEIVED BY MANUFACTURER.

    Description of Event or Problem · 1

    STRETCHER LEGS DID NOT LOCK WHILE ATTENDANTS WERE ATTEMPTING TO UNLOAD A (B) (6) TO (B) (6) POUND PT FROM THE AMBULANCE. ONE EMT REPORTED INJURY TO FINGERS ON HER LEFT HAND, LOWER BACK AND LEFT FOOT. EMT REPORTED SHE DID NOT FEEL SHE NEEDED TO SEEK MEDICAL ATTENTION.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 FERNO PROFLEXX 35X AMBULANCE STRETCHER FERNO PROFLEXX 35X AMBULANCE STRETCHER FPO FERNO-WASHINGTON, INC.

    Patients

    Seq Age Sex Outcome Treatment
    1 31 YR Other