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Data Cable 1575Recalls & reported problems

Heartware Inc. · Class 3 · Implant

2 open recalls name this device. See the recall details and contact the manufacturer or your healthcare provider.

Adverse event reports
0
Deaths reported
0
Injuries reported
0
Recalls naming it
2

Summary

No MAUDE adverse event reports in our data reference this device identifier directly.

2 FDA recall records name this device's identifier, 2 still open.

58 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.

Recalls naming this device

  1. Feb 26, 2021Open, Classified

    IFU and Patient Manual updated to describe Expected Alarm Duration. The Instructions for Use (IFU) is being updated to advise clinicians that alarms that resolve after a very short period may mean there is an intermittent problem and the cause of the alarm can be evaluated by analysis of the controller log files. The Patient Manual (PM) is being updated to instruct patients to contact their clinicians if they cannot identify an alarm before it is cleared as it might mean there is an intermittent problem. NOTE: this update is included in the February 2021 Urgent Medical Device Notice also covered in recalls 87456 and 87604

    Z-1469-2021 · Root cause: Device Design · FDA record ↗

  2. Feb 26, 2021Open, Classified

    IFU and Patient Manual updated to describe HVAD Controller Connection Verification. The labeling is being corrected to reflect the actual verified behavior of a successful connector to the controller, which is a "beep" and not "audible click", to clarify under what alarm conditions a beep will not be heard, and identify alternate confirmation methods (visual indicator) for successful connection. NOTE: this update is included in the February 2021 Urgent Medical Device Notice also covered in recalls 87456 and 87603

    Z-1438-2021 · Root cause: Device Design · FDA record ↗

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-1102-2022 · Mar 30, 2022 · Open, Classified
    HeartWare Ventricular Assist Device (HVAD) System, Pump Implant Kit, Model Number1104
  • 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-1103-2022 · Mar 30, 2022 · Open, Classified
    HeartWare Ventricular Assist Device (HVAD) System Controller, Model Number 1407DE Kit
  • Z-1105-2022 · Mar 30, 2022 · Open, Classified
    HeartWare Ventricular Assist Device (HVAD) System Controller, Model Number 1420-Controller 2.0
  • Z-1104-2022 · Mar 30, 2022 · Open, Classified
    HeartWare Ventricular Assist Device (HVAD) System Controller, Model Number 1420
  • 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-1106-2022 · Mar 30, 2022 · Open, Classified
    HeartWare Ventricular Assist Device (HVAD) System, Model Number 1521DE, MONITOR 1521DE EXPLORE TECH
  • 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-2191-2021 · Jun 3, 2021 · Open, Classified
    HeartWare HVAD Pump Implant Kit, REF 1153

…and 43 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.