BEUDAMED
    FDA Adverse Event Summary report: N

    CADD-PLUS PUMP

    MDR report key: 33167 · Received May 23, 1996

    Report

    Report Number
    MW1009150
    Date Received
    May 23, 1996
    Date of Event
    May 16, 1996
    Report Date
    May 21, 1996
    Manufacturer
    PHARMACIA DELTEC, INC.
    Product Code
    FRN
    Adverse Event
    Yes
    Report Source
    Voluntary report
    Reporter Location
    CA, US
    Reporter Occupation
    PHARMACIST

    Narratives

    Description of Event or Problem · 1

    LOCK LEVEL MECHANISM FAILED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 CADD-PLUS PUMP INFUSION PUMP FRN PHARMACIA DELTEC, INC. 5400

    Patients

    Seq Age Sex Outcome Treatment
    1 NO INFO