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, ClassifiedHVAD (HeartWare Ventricular Assist Device) STERILE IMPLANT KIT, Model Number 1100
- Z-1993-2023 · May 16, 2023 · Open, ClassifiedHeartWare 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, ClassifiedHeartWare Ventricular Assist Device (HVAD) System Batteries, Product Number 1650DE
- Z-1266-2022 · May 5, 2022 · Open, ClassifiedHeartWare Battery, Model #1650DE, a component of the HeartWare Ventricular Assist Device (HVAD) System.
- Z-1207-2022 · Apr 14, 2022 · Open, ClassifiedHeartWare HVAD Pump Implant Kit, a) Model Number 1104JP, b) Model Number MCS1705PU
- Z-1106-2022 · Mar 30, 2022 · Open, ClassifiedHeartWare Ventricular Assist Device (HVAD) System, Model Number 1521DE, MONITOR 1521DE EXPLORE TECH
- Z-1102-2022 · Mar 30, 2022 · Open, ClassifiedHeartWare Ventricular Assist Device (HVAD) System, Pump Implant Kit, Model Number1104
- Z-1110-2022 · Mar 30, 2022 · Open, ClassifiedInstructions 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, ClassifiedHeartWare Ventricular Assist Device (HVAD) System Controller, Model Number 1420-Controller 2.0
- Z-1103-2022 · Mar 30, 2022 · Open, ClassifiedHeartWare Ventricular Assist Device (HVAD) System Controller, Model Number 1407DE Kit
- Z-1107-2022 · Mar 30, 2022 · Open, ClassifiedHeartWare 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, ClassifiedHeartWare Ventricular Assist Device (HVAD) System Controller, Model Number 1420
- Z-0726-2022 · Jan 27, 2022 · Open, ClassifiedHeartWare Ventricular Assist Device (HVAD) System
- Z-2478-2021 · Aug 6, 2021 · Open, ClassifiedMedtronic HVAD Pump Implant Kits
- Z-2196-2021 · Jun 3, 2021 · Open, ClassifiedHeartWare HVAD Outflow Graft, REF MCS1725OG
…and 45 more.
Other Ventricular (Assist) Bypass devices
- Thoratec® HeartMate 3™ 106524USThoratec Corporation · Ventricular (Assisst) Bypass7 recalls5,096 deaths16,478 reports
- THORATEC® HEARTMATE®, LVAS IMPLANT KIT (WITH SEALED GRAFTS) 106015Thoratec Corporation · Ventricular (Assisst) Bypass2 recalls2,141 deaths8,000 reports
- Thoratec® HeartMate 3™ 106531USThoratec Corporation · Ventricular (Assisst) Bypass1 recall11 deaths4,646 reports
- HVAD Pump Implant Kit 1103Heartware Inc. · Ventricular (Assist) Bypass6 recalls424 deaths2,952 reports
- HVAD® Pump Implant Kit (Enhanced) 1103Heartware Inc. · Ventricular (Assisst) Bypass4 recalls573 deaths2,807 reports
- HVAD® Pump Implant Kit 1103Heartware Inc. · Ventricular (Assisst) Bypass4 recalls666 deaths2,737 reports
- HVAD® Controller 1420Heartware Inc. · Ventricular (Assisst) Bypass5 recalls14 deaths2,161 reports
- HEARTMATE®, MOBILE POWER UNIT, NA 107754Thoratec Corporation · Ventricular (Assisst) Bypass1 death2,098 reports
Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.