BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    CADD PLUS IV PUMP

    MDR report key: 213089 · Received March 4, 1999

    Report

    Report Number
    MW1015837
    Event Type
    Malfunction
    Date Received
    March 4, 1999
    Date of Event
    February 19, 1999
    Report Date
    February 26, 1999
    Manufacturer
    SIMS DELTEC, INC.
    Product Code
    FRN
    Product Problem
    Yes
    Report Source
    Voluntary report
    Reporter Location
    CT, US
    Reporter Occupation
    NURSE

    Narratives

    Description of Event or Problem · 1

    CADD PLUS PUMP DISPLAYED "99 LOW BATTERY". NEW BATTERY HAD BEEN USED. STARTED PUMP IN "LLI". RESIDUAL VOLUME DISPLAYED 580. ONCE IN START MODE THE PUMP SWITCHED TO "99 LOW BATTERY". VISITING NURSE REQUESTED AND REC'D NEW CADD PLUS WHICH WORKED CORRECTLY.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 CADD PLUS IV PUMP IV PUMP FRN SIMS DELTEC, INC. UNK UNK

    Patients

    Seq Age Sex Outcome Treatment
    1 * Other