BEUDAMED
    FDA Adverse Event Injury Summary report: N

    MEDI-VAC CRD HARDWARE

    MDR report key: 474861 · Received July 24, 2003

    Report

    Report Number
    MW1029141
    Event Type
    Injury
    Date Received
    July 24, 2003
    Date of Event
    May 29, 2003
    Manufacturer
    CARDINAL HEALTH, INC.
    Product Code
    GCY
    Adverse Event
    Yes
    Product Problem
    Yes
    Report Source
    Voluntary report
    Reporter Location
    CA, US
    Reporter Occupation
    RISK MANAGER

    Narratives

    Description of Event or Problem · 1

    CONCERN THAT SWITCH ON BACK OF CANISTER HOLDER IS AT THE BACK OF THE UNIT AND DIFFICULT TO SEE. RPTR QUESTIONS IF THE PRESENCE OF THIS SWITCH IS OF SIGNIFICANT IMPORTANCE THAT THE RISK OF IT BEING OVERLOOKED IS NEGATED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 MEDI-VAC CRD HARDWARE SUCTION CANISTER HOLDER GCY CARDINAL HEALTH, INC. 65652-516 NA

    Patients

    Seq Age Sex Outcome Treatment
    1 70 YR