BEUDAMED
    FDA Adverse Event Summary report: N

    PHARMAACIA DELTEC

    MDR report key: 15742 · Received January 27, 1994

    Report

    Report Number
    1422558-1993-09008
    Date Received
    January 27, 1994
    Date of Event
    November 11, 1993
    Report Date
    November 21, 1993
    Manufacturer
    PHARMACIA DELTEC, INC.
    Product Code
    LHI
    Report Source
    Distributor report

    Narratives

    Description of Event or Problem · 1

    AT 9:30 AM RN INFORMS THAT PT DIED OF CARDIAC ARREST IN HIS SLEEP. PHONE CALL WAS RECEIVED FROM MANUFACTURER REQUESTING WE SEND PUMP TO THEM, BECAUSE THE PT WHO HAD IT DIED TODAY AND MFG WANTED TO EXAMINE THE PUMP.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 PHARMAACIA DELTEC CADD PLUS I.V. PUMP LHI PHARMACIA DELTEC, INC. CADD PLUS

    Patients

    Seq Age Sex Outcome Treatment
    1 *