BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    WALKMED 350VL INFUSION PUMP

    MDR report key: 25151363 · Received May 12, 2026

    Report

    Report Number
    MW5188041
    Event Type
    Malfunction
    Date Received
    May 12, 2026
    Date of Event
    May 6, 2026
    Report Date
    May 7, 2026
    Manufacturer
    WALKMED TECHNOLOGIES, LLC.
    Product Code
    FRN
    Product Problem
    Yes
    Report Source
    Voluntary report
    Reporter Location
    KS, US
    Reporter Occupation
    OTHER HEALTH CARE PROFESSIONAL
    Health Professional
    *

    Narratives

    Description of Event or Problem · 0

    PATIENT CAME IN FOR APPOINTMENT TO REMOVE CADD(CONTINUOUS AMBULATORY DELIVERY DEVICE) PUMP AND DEACCESS PORT. PUMP REPORTED INFUSION COMPLETED. UPON REMOVING CHEMO BAG OUT OF PUMP, KELLY RN NOTICED THERE WAS APPROXIMATELY 2/3 OF THE MEDICATION STILL REMAINING IN BAG. DR CANNON WAS NOTIFIED OF INCIDENT AND GAVE VERBAL ORDER TO DC(DISCONTINUED) REMAINING MEDICATION. DEFAULTY PUMP WILL BE MAILED BACK TO INFUSYSTEM, AND INFUSYSTEM MEMBER WAS NOTIFIED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    611177 WALKMED 350VL INFUSION PUMP PUMP, INFUSION FRN WALKMED TECHNOLOGIES, LLC. WALKMED 350VL

    Patients

    Seq Age Sex Outcome Treatment
    1 50 YR Male