BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    FERNO PRO FLEX 35-P

    MDR report key: 1103423 · Received August 7, 2008

    Report

    Report Number
    MW5007930
    Event Type
    Malfunction
    Date Received
    August 7, 2008
    Report Date
    August 7, 2008
    Manufacturer
    FERNO-WASHINGTON
    Product Code
    FPO
    Product Problem
    Yes
    Report Source
    Voluntary report
    Reporter Location
    MA, US
    Reporter Occupation
    NURSE

    Narratives

    Description of Event or Problem · 1

    EIGHT AMBULANCE STRETCHERS WERE TAKEN OUT OF SERVICE DUE TO FRAME FRACTURED, FERNO STRETCHERS PRO FLEX 35-P. NO KNOWN PATIENT INJURY. SAME SER # ON ALL DEVICES.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 FERNO PRO FLEX 35-P FERNO AMBULANCE STRETCHER FPO FERNO-WASHINGTON FERNO PRO FLEX 35-P
    2 FERNO PRO FLEX 35-P FERNO AMBULANCE STRETCHER FPO FERNO-WASHINGTON FERNO PRO FLEX 35-P
    3 FERNO PRO FLEX 35-P FERNO AMBULANCE STRETCHER FPO FERNO-WASHINGTON FERNO PRO FLEX 35-P
    4 FERNO PRO FLEX 35-P FERNO AMBULANCE STRETCHER FPO FERNO-WASHINGTON FERNO PRO FLEX 35-P
    5 FERNO PRO FLEX 35-P FERNO AMBULANCE STRETCHER FPO FERNO-WASHINGTON FERNO PRO FLEX 35-P
    6 FERNO PRO FLEX 35-P FERNO AMBULANCE STRETCHER FPO FERNO-WASHINGTON FERNO PRO FLEX 35-P
    7 FERNO PRO FLEX 35-P FERNO AMBULANCE STRETCHER FPO FERNO-WASHINGTON FERNO PRO FLEX 35-P
    8 FERNO PRO FLEX 35-P FERNO AMBULANCE STRETCHER FPO FERNO-WASHINGTON FERNO PRO FLEX 35-P

    Patients

    Seq Age Sex Outcome Treatment
    1