BEUDAMED
    FDA Adverse Event Other Summary report: N

    CAREFUSION

    MDR report key: 3727656 · Received March 28, 2014

    Report

    Report Number
    MW5035446
    Event Type
    Other
    Date Received
    March 28, 2014
    Date of Event
    March 11, 2014
    Report Date
    March 27, 2014
    Manufacturer
    CAREFUSION
    Product Code
    FPA
    Report Source
    Voluntary report
    Reporter Location
    IL, US
    Reporter Occupation
    NURSE

    Narratives

    Description of Event or Problem · 1

    AN EPIDURAL CATHETER WAS INSERTED IN PT BY THE ANESTHESIOLOGIST. NURSING STAFF USED PCA TUBING, RATHER THAN EPIDURAL TUBING, TO CONNECT EPIDURAL CATHETER TO INFUSION PUMP. ERROR WAS DETECTED THE FOLLOWING DAY. NO HARM OR IMPACT TO PT.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    184986 CAREFUSION TUBING FPA CAREFUSION

    Patients

    Seq Age Sex Outcome Treatment
    1 83 YR ALARIS INFUSION PUMP