BEUDAMED
    FDA Adverse Event Injury Summary report: N

    MOOG CURLIN MEDICAL PAIN SMART IOD

    MDR report key: 1962564 · Received January 11, 2011

    Report

    Report Number
    MW5018987
    Event Type
    Injury
    Date Received
    January 11, 2011
    Date of Event
    January 11, 2011
    Report Date
    January 11, 2011
    Manufacturer
    MOOG MEDICAL DEVICES GROUP
    Product Code
    FRN
    Product Problem
    Yes
    Report Source
    Voluntary report
    Reporter Location
    NJ, US
    Reporter Occupation
    RISK MANAGER

    Narratives

    Description of Event or Problem · 1

    MOOG CURLIN MEDICAL PAIN SMART IOD PUMPS HAVE FAULTY POWER CORDS. THE ELECTRICAL PRONGS SEPARATE FROM THE POWER BOX AND CAN BE RETAINED IN THE WALL. THE POWER BOX ALSO SEPARATES EASILY, EXPOSING THE ELECTRONIC COMPONENTS. THE PUMP CONVERTS TO BATTERY POWER SO THE PT IS NOT COMPROMISED BUT THE CORD FAILURE PRESENTS A SAFETY CONCERN FOR STAFF. DATES OF USE: SINCE (B)(6) 2010.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 MOOG CURLIN MEDICAL PAIN SMART IOD PCA PUMP FRN MOOG MEDICAL DEVICES GROUP 92649

    Patients

    Seq Age Sex Outcome Treatment
    1 NA Required Intervention