BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    ALTERNATING LEG PRESSURE VENOUS THROMBOEMBOLISM PREVENTION S

    MDR report key: 770804 · Received October 4, 2006

    Report

    Report Number
    770804
    Event Type
    Malfunction
    Date Received
    October 4, 2006
    Date of Event
    September 24, 2006
    Report Date
    September 29, 2006
    Manufacturer
    CURRIE MEDICAL SPECIALTIES, INC.
    Product Code
    JOW
    Product Problem
    Yes
    Report Source
    User Facility report
    Reporter Location
    CA, US

    Narratives

    Description of Event or Problem · 1

    PNEUMATIC COMPRESSION DEVICE ATTACHED TO SCD STOCKING/BOOTS ON PATIENT AND THE MACHINE STARTED TO BEEP. RECHECKED ALL CABLES AND COULD TELL THAT THE SCD STOCKINGS/BOOTS WERE NOT FILLING UP.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 ALTERNATING LEG PRESSURE VENOUS THROMBOEMBOLISM PREVENTION S PNEUMATIC COMPRESSION DEVICE JOW CURRIE MEDICAL SPECIALTIES, INC. ALP501 *

    Patients

    Seq Age Sex Outcome Treatment
    1 *