BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    SPECTRUM INFUSION PUMP

    MDR report key: 3060544 · Received March 27, 2013

    Report

    Report Number
    1314492-2013-00307
    Event Type
    Malfunction
    Date Received
    March 27, 2013
    Date of Event
    February 26, 2013
    Report Date
    February 26, 2013
    Manufacturer
    BAXTER HEALTHCARE CORP
    Product Code
    FRN
    PMA / PMN Number
    K042121
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    PA, US
    Reporter Occupation
    NURSE

    Narratives

    Additional Manufacturer Narrative · 1

    (B)(4). BAXTER IS CONTINUING TO INVESTIGATE THE REPORTED EVENT.

    Description of Event or Problem · 1

    IT WAS REPORTED THAT A PUMP ALARMED FOR "UPSTREAM OCCLUSION!" WHEN NO UPSTREAM OCCLUSION WAS PRESENT. THE ALARM OCCURRED IN THE SICU DURING AN INFUSION OF VASOPRESSIN AT A RATE OF 9 ML/HR. IT WAS REPORTED THAT THE SOLUTION INFUSING WAS ROOM TEMPERATURE. IT WAS ALSO REPORTED "HEAD HEIGHT TERRIBLE, LESS THAN 6 INCHES, NO TUBING KINKS OR ABNORMALITIES." IT WAS ALSO REPORTED THAT THERE WAS NO PT INJURY.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    127120 SPECTRUM INFUSION PUMP INFUSION PUMP FRN BAXTER HEALTHCARE CORP 35700

    Patients

    Seq Age Sex Outcome Treatment
    1