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Thoratec® HeartMate 3™ 106532USRecalls & reported problems

Thoratec Corporation · Thread Protectors · Class 3

All models of Thoratec HeartMate 3 (9)

Data updated Oct 18, 2026 from official FDA records · Editorial policy

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 05415067030818), received between Oct 18, 2018 and Oct 18, 2018 — classified as 1 malfunction.

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

18 other recalls cover devices cleared under the same FDA submission (P160054); 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. What reports can and can't tell you · How this data works · Data updated Oct 18, 2026.

Most reported problems

Device problems

  • Break1
  • Detachment of Device or Device Component1
  • Difficult to Remove1

Patient problems

  • No Known Impact Or Consequence To Patient1

Recent adverse event reports

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

  • MalfunctionOct 18, 2018Break; Difficult to Remove; Detachment of Device or Device Component; Break; Difficult to Remove; Detachment of Device or Device Component

    THE PATIENT WAS IMPLANTED WITH A LEFT VENTRICULAR ASSIST DEVICE (LVAD). IT WAS REPORTED, THAT DURING PROCEDURE ON (B)(6) 2018, THE SURGEON WAS PASSING THE TUNNELLER TO PULL DRIVELINE THROUGH THE PATIENT¿S BODY HABITUS, WHEN A BLACK SEGMENT OF THE TUNNELER ADAPTOR BROKE OFF. THE TUNNELING ADAPTER WILL BE RETURNED FOR FURTHER EVALUATION. THE PUMP WAS PLACED WITHOUT ISSUES AND FUNCTIONED AS INTENDED NO FURTHER INFORMATION WAS PROVIDED.

    Patient problems: No Known Impact Or Consequence To Patient

    MAUDE report 7980976 ↗

Recalls under the same FDA submission

These recalls involve devices cleared under P160054. One submission often covers many models, so check the product and lot details in each record.

  • Z-2519-2026 · May 13, 2026 · Open, Classified
    Brand Name: HeartMate Product Name: HeartMate 3" System Controller Model/Catalog Number: 106531US Software Version: N/A Product Description: The HeartMate 3" System Controller acts
  • Z-2518-2026 · May 13, 2026 · Open, Classified
    Brand Name: HeartMate Product Name: HeartMate 3 Left Ventricular System (LVAS) Kits Model/Catalog Number: 106524US Software Version: N/A Product Description: The HeartMate 3" Left
  • Z-2520-2026 · May 13, 2026 · Open, Classified
    Brand Name: HeartMate Product Name: HM 11V Li-ion Backup Battery, ABT Model/Catalog Number: 106128 Software Version: N/A Product Description: The HeartMate 11 Volt Lithium Ion Stan
  • Z-0505-2026 · Oct 9, 2025 · Open, Classified
    Brand Name: HeartMate Product Name: HeartMate 3 Left Ventricular System (LVAS) Kits Model/Catalog Number: 106524US, HeartMate 3 LVAS KIT, US; 106524INT, HeartMate 3 LVAD KIT, OUS
  • Z-0506-2026 · Oct 9, 2025 · Open, Classified
    Brand Name: HeartMate Product Name: HeartMate 3 Controller (Standalone) Model/Catalog Number: 106531US, HeartMate 3 Controller, US; 106531INT, HeartMate 3 Controller, OUS; 106531
  • Z-2290-2025 · Jun 23, 2025 · Open, Classified
    Brand Name: HeartMate Product Name: Mobile Power Unit, AC Power Cord Model/Catalog Number: 107760 Software Version: N/A Product Description: The HeartMate 3" Left Ventricular Assis
  • Z-2291-2025 · Jun 23, 2025 · Open, Classified
    Brand Name: HeartMate Product Name: Mobile Power Unit Model/Catalog Number: 107754 Software Version: N/A Product Description: The HeartMate 3" Left Ventricular Assist System (LVAS)
  • Z-1570-2025 · Mar 13, 2025 · Open, Classified
    HeartMate Mobile Power Unit: REF: 107754, NA; 107758, EU; 107758AU, AU; 107758UK, UK; L107758, EU Rental. Used with HeartMate 3 and II Left Ventricular Assist System.
  • Z-2583-2024 · Jun 25, 2024 · Open, Classified
    HeartMate 3 System Controllers provided within the following HeartMate 3 Left Ventricular Assist System (LVAS) Implant Kits or distributed separately: HeartMate 3 LVAS Implant Ki
  • Z-1921-2024 · May 8, 2024 · Open, Classified
    Thoratec HeartMate System Monitor, REF: 1286, L1286, 1286A, L1286A, 1286A-US, L1286A-US, 1286C, L1286C, L1386, 1286A-CAN, 1286INT and L1286INT. Left ventricular assist device
  • Z-1693-2024 · Mar 1, 2024 · Open, Classified
    Thoratec HeartMate 3, LVAS Implant Kit, REF:106524INT, Sterile EO, RxOnly
  • Z-1692-2024 · Mar 1, 2024 · Open, Classified
    Thoratec HeartMate 3, LVAS Implant Kit, REF:106524US, Sterile EO, RxOnly
  • Z-1301-2024 · Feb 19, 2024 · Open, Classified
    HeartMate 3 Left Ventricular Assist System (LVAS): 1. HeartMate 3 Sealed Outflow Graft with Bend Relief, Investigational Device Exemption (IDE) 2. HeartMate 3 Sealed Outflow Graf
  • Z-0842-2024 · Jan 3, 2024 · Open, Classified
    1. HeartMate Touch Communication System, REF HMT1100 2. HeartMate Touch Communication System, Rental REF HMT1100-R 3. HeartMate Touch Communication System, HMT1150 The HeartMate T
  • Z-0746-2020 · Dec 2, 2019 · Terminated
    HeartMate 3 Mobile Power Unit, REF 107754, UDI or GTIN: 00813024010883, and 107758, UDI or GTIN: 00813024010890, when connected to the HeartMate 3 Left Ventricular Assist System, R

…and 3 more.

Other Ventricular (assist) bypass devices

All Ventricular (assist) bypass devices →

Sources and updates

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