BEUDAMED
    FDA Adverse Event Summary report: N

    FU PUMP

    MDR report key: 10263521 · Received July 10, 2020

    Report

    Report Number
    MW5095491
    Date Received
    July 10, 2020
    Report Date
    July 10, 2020
    Manufacturer
    WALKMED, LLC
    Product Code
    FRN
    Report Source
    Voluntary report
    Reporter Occupation
    UNKNOWN

    Narratives

    Description of Event or Problem · 1

    DESCRIPTION: FU PUMP WAS PROGRAMMED WRONG IN THE WALKMED PUMP. DECIMAL POINT LOCATION VARIES FROM PUMP TO PUMP. RATE WAS ENTERED AS 20MG/HR INSTEAD OF 2ML/HR. PATIENT WAS ADMITTED TO HOSPITAL VISTOGARD X 20 DOSES GIVEN TO PATIENT. (B)(6).

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    722391 FU PUMP PUMP, INFUSION FRN WALKMED, LLC

    Patients

    Seq Age Sex Outcome Treatment
    1