BEUDAMED
    FDA Adverse Event Injury Summary report: N

    BARD PCA PUMP

    MDR report key: 29342 · Received January 2, 1996

    Report

    Report Number
    29342
    Event Type
    Injury
    Date Received
    January 2, 1996
    Date of Event
    December 18, 1995
    Report Date
    December 28, 1995
    Manufacturer
    BARD MEDSYSTEMS DIV. C.R. BARD, INC.
    Product Code
    MEA
    Product Problem
    Yes
    Report Source
    User Facility report
    Reporter Location
    ME, US
    Reporter Occupation
    PHARMACIST

    Narratives

    Description of Event or Problem · 1

    PCA PUMP INFUSION WAS STARTED ON 12/14. ON 12/17 2200 BAG WAS CHANGED AND FLUID REMAINING IN BAG WAS MEASURED TO BE APPROXIMATELY 45 ML AND PUMP HISTORY STATED 7 ML REMAINING. CO WAS CALLED AND CO STATED THAT NO ALARM WILL GO OFF IF TUBING IS OCCLUDED BEFORE PERISTALTIC DEVICE AND PUMP WILL REGISTER AN "ACCURATE" INFUSION.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 BARD PCA PUMP PCA PUMP MEA BARD MEDSYSTEMS DIV. C.R. BARD, INC. 6465441

    Patients

    Seq Age Sex Outcome Treatment
    1 69 YR Required Intervention