BEUDAMED
    FDA Adverse Event Injury Summary report: N

    HEARTMATE 3 MPU

    MDR report key: 23927133 · Received December 30, 2025

    Report

    Report Number
    23927133
    Event Type
    Injury
    Date Received
    December 30, 2025
    Date of Event
    February 11, 2025
    Report Date
    February 12, 2025
    Manufacturer
    ABBOTT
    Product Code
    DSQ
    Product Problem
    Yes
    Report Source
    User Facility report
    Reporter Location
    NC, US
    Reporter Occupation
    NURSE
    Health Professional
    Yes

    Narratives

    Description of Event or Problem · 0

    PATIENT ARRIVED TO CLINIC ON (B)(6) 2025 FOR PROBLEM VISIT REGARDING MOBILE POWER UNIT (MPU). MPU WITH KINK IN THE POWER CORD AND UNIT ALARMS WHEN CONNECTED TO WALL POWER. MPU REPLACED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    2638628 HEARTMATE 3 MPU LEFT VENTRICULAR ASSIST DEVICE DSQ ABBOTT

    Patients

    Seq Age Sex Outcome Treatment
    1 56 YR Male Required Intervention