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HeartWare® Controller DC Adapter 1440 (UDI 00888707009935)Recalls & reported problems

Heartware Inc. · Class 3 · Implant

Adverse event reports
1
Deaths reported
0
Injuries reported
0
Recalls naming it
0

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00888707009935), received between May 25, 2023 and May 25, 2023 — classified as 1 malfunction.

The most frequently reported specific device problem is “Power Problem” (1 report).

60 other recalls cover devices cleared under the same FDA submission (P100047); they may or may not involve this specific model.

Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event, and counts can't be used to compare devices or estimate failure rates. How this data works · Data updated Oct 13, 2026.

Most reported problems

Device problems

  • Power Problem1

Patient problems

  • No Clinical Signs, Symptoms or Conditions1

Recent adverse event reports

The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.

  • MalfunctionMay 25, 2023Power Problem; Power Problem

    IT WAS REPORTED THAT THE CONTROLLER ADAPTER (CDC) DOES NOT PROVIDE POWER. THE CDC WILL BE REPLACED. NO PATIENT COMPLICATIONS HAVE BEEN REPORTED AS A RESULT OF THIS EVENT.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 17004879 ↗

Recalls under the same FDA submission

These recalls involve devices cleared under P100047. One submission often covers many models, so check the product and lot details in each record.

  • Z-0475-2024 · Oct 31, 2023 · Open, Classified
    HVAD (HeartWare Ventricular Assist Device) STERILE IMPLANT KIT, Model Number 1100
  • Z-1993-2023 · May 16, 2023 · Open, Classified
    HeartWare Ventricular Assist Device System. a) Monitor 1521US Explore Tech, b) Monitor 1521GB Explore Tech, c) Monitor 1521IL Explore Tech, d) Monitor 1521DE Explore Tech
  • Z-1512-2022 · Jun 28, 2022 · Open, Classified
    HeartWare Ventricular Assist Device (HVAD) System Batteries, Product Number 1650DE
  • Z-1266-2022 · May 5, 2022 · Open, Classified
    HeartWare Battery, Model #1650DE, a component of the HeartWare Ventricular Assist Device (HVAD) System.
  • Z-1207-2022 · Apr 14, 2022 · Open, Classified
    HeartWare HVAD Pump Implant Kit, a) Model Number 1104JP, b) Model Number MCS1705PU
  • Z-1106-2022 · Mar 30, 2022 · Open, Classified
    HeartWare Ventricular Assist Device (HVAD) System, Model Number 1521DE, MONITOR 1521DE EXPLORE TECH
  • Z-1102-2022 · Mar 30, 2022 · Open, Classified
    HeartWare Ventricular Assist Device (HVAD) System, Pump Implant Kit, Model Number1104
  • Z-1110-2022 · Mar 30, 2022 · Open, Classified
    Instructions for Use, Patient Manuals, and Emergency Responder Guides for HeartWare Ventricular Assist Device (HVAD) System. HVAD System. IFUs are distributed as part of the Pump
  • Z-1105-2022 · Mar 30, 2022 · Open, Classified
    HeartWare Ventricular Assist Device (HVAD) System Controller, Model Number 1420-Controller 2.0
  • Z-1103-2022 · Mar 30, 2022 · Open, Classified
    HeartWare Ventricular Assist Device (HVAD) System Controller, Model Number 1407DE Kit
  • Z-1107-2022 · Mar 30, 2022 · Open, Classified
    HeartWare Ventricular Assist Device (HVAD) System, individual pamphlets: HVAD System Emergency Responder Guide (FI-Finnish) HVAD System Emergency Responder Guide (FI-Finnish) H
  • Z-1104-2022 · Mar 30, 2022 · Open, Classified
    HeartWare Ventricular Assist Device (HVAD) System Controller, Model Number 1420
  • Z-0726-2022 · Jan 27, 2022 · Open, Classified
    HeartWare Ventricular Assist Device (HVAD) System
  • Z-2478-2021 · Aug 6, 2021 · Open, Classified
    Medtronic HVAD Pump Implant Kits
  • Z-2196-2021 · Jun 3, 2021 · Open, Classified
    HeartWare HVAD Outflow Graft, REF MCS1725OG

…and 45 more.

Other Ventricular (Assist) Bypass devices

All Ventricular (Assist) Bypass devices →

Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.