Thoratec LLC recalls
Every recall we track for Thoratec LLC — 12 in all, from 2024–2026 — plus the complaints and injury reports the public filed about them.
Recalls per year, by danger level
Recalls from Thoratec LLC more than tripled in 2025 (8, up from 1 in 2024).
All FDA recall records for Thoratec LLC since 2017, counted by recall date (one bar per calendar year; 2026 is partial). Danger level is GovInfoNow’s plain-language rating; “not yet rated” records are still being written up.
| Year | Stop using now | Use caution | Lower risk | Not yet rated | Total |
|---|---|---|---|---|---|
| 2017 | 0 | 0 | 0 | 0 | 0 |
| 2018 | 0 | 0 | 0 | 0 | 0 |
| 2019 | 0 | 0 | 0 | 0 | 0 |
| 2020 | 0 | 0 | 0 | 0 | 0 |
| 2021 | 0 | 0 | 0 | 0 | 0 |
| 2022 | 0 | 0 | 0 | 0 | 0 |
| 2023 | 0 | 0 | 0 | 0 | 0 |
| 2024 | 0 | 1 | 0 | 0 | 1 |
| 2025 | 0 | 5 | 2 | 1 | 8 |
| 2026 (to date) | 0 | 0 | 1 | 2 | 3 |
Most common reasons for Thoratec LLC recalls
What to do if you have a recalled Thoratec LLC product
- Match the model, catalog or lot number on your device to the recall.
- Ask the prescribing clinician or supplier what to do — many device recalls are corrections, not removals.
- Report problems to FDA MedWatch.
All Thoratec LLC recalls
6 shown- Lower riskMedical device
Thoratec LLC recalls Brand Name: HeartMate Product Name: HeartMate 3" System Controller Model/Catalog Number: 106531US Software Version: N/A
Thoratec recalls HeartMate 3 System Controller (model 106531US) due to potential 11-volt backup battery failures. Affected users should contact for remedy.
HeartMateMay 13, 2026 - Use cautionMedical device
Thoratec LLC recalls CentriMag Blood Pump, REF: 102953, 201-20003, 201-90010, 201-90016; CentriMag RVAD HDE KIT, REF: 104318; CentriMag
Thoratec recalls CentriMag Blood Pumps (REFs 102953, 201-20003, 201-90010, 201-90016) and CentriMag RVAD HDE KIT (REF 104318) due to risk of pump not securely locking into motor, which could cause particulate, heat, or serious complications.
ThoratecOct 10, 2025 - Lower riskMedical device
Thoratec LLC recalls Brand Name: HeartMate Product Name: HeartMate 3 Controller (Standalone) Model/Catalog Number: 106531US, HeartMate 3
Thoratec recalls HeartMate 3 Controller models due to potential corrosion in backup battery cable connector causing fault alarms. Affected units may need replacement of backup battery.
HeartMateOct 9, 2025 - Use cautionMedical device
Thoratec LLC recalls Brand Name: HeartMate Product Name: Mobile Power Unit, AC Power Cord Model/Catalog Number: 107760 Software Version: N/A
HeartMate recalls Mobile Power Unit AC Power Cord model 107760 due to misaligned V-Lock feature causing unintended disconnect. Affected patients should check if their device uses this model.
HeartMateJun 23, 2025 - Use cautionMedical device
Thoratec LLC recalls HeartMate Mobile Power Unit: REF: 107754, NA; 107758, EU; 107758AU, AU; 107758UK, UK; L107758, EU Rental. Used with
Thoratec recalls HeartMate Mobile Power Units (MPUs) with serial numbers from 20226263 to 20307999. These units may experience electrical issues causing unintended shutdowns or alarms. If power is lost, the system may run for up to 15 minutes before stopping. Affected units were distributed between April 2024 and February 2025.
ThoratecMar 13, 2025 - Use cautionMedical device
Thoratec LLC recalls HeartMate 3 System Controllers provided within the following HeartMate 3 Left Ventricular Assist System (LVAS) Implant
Thoratec recalls HeartMate 3 System Controllers with specific model numbers and serials due to risk of fluid exposure causing false alarms and system failure. Affected units include certain HeartMate 3 LVAS Implant Kits and controllers.
ThoratecJun 25, 2024
Thoratec LLC recall questions
How many recalls has Thoratec LLC had?
12 recalls from Thoratec LLC are on record with U.S. safety agencies, from 2024–2026.
What is the most recent Thoratec LLC recall?
Thoratec LLC recalls Brand Name: HeartMate Product Name: HeartMate 3" System Controller Model/Catalog Number: 106531US Software Version: N/A, dated May 13, 2026. Every Thoratec LLC recall is listed on this page, newest first.
Why are Thoratec LLC products recalled?
The most common reasons on record: Due to 11 volt Backup Battery failures. (3).
What should I do if I have a recalled Thoratec LLC product?
Match the model, catalog or lot number on your device to the recall. Ask the prescribing clinician or supplier what to do — many device recalls are corrections, not removals. Report problems to FDA MedWatch.
How do I get alerts for new Thoratec LLC recalls?
Sign up for free email alerts on GovInfoNow — we check official CPSC, FDA, USDA and NHTSA data every day and email you only when a recall matches what you follow.