BEUDAMED
    FDA Adverse Event Injury Summary report: N

    HEARTMATE 3

    MDR report key: 23760229 · Received December 9, 2025

    Report

    Report Number
    23760229
    Event Type
    Injury
    Date Received
    December 9, 2025
    Date of Event
    December 10, 2024
    Report Date
    February 4, 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) 2024 FOR AN EQUIPMENT CHECK. MODULAR CABLE NOTED WITH MULTIPLE TEARS REPAIRED WITH MEDICAL TAPE. MODULAR CABLE REPLACED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    2885249 HEARTMATE 3 LEFT VENTRICULAR ASSIST DEVICE CABLE DSQ ABBOTT

    Patients

    Seq Age Sex Outcome Treatment
    1 25 YR Male Required Intervention