Go Backs
HomeCategoriesStatesCheck Your Home
Go Backs

Track product recalls and safety alerts from CPSC, FDA, NHTSA, and USDA. Stay informed and keep your family safe.

Browse

  • Categories
  • States
  • Check Your Home
  • Risk Levels

Agencies

  • CPSC
  • FDA Food
  • FDA Drug
  • FDA Device
  • FDA Veterinary
  • NHTSA
  • USDA

Company

  • About
  • FAQ
  • Contact
  • Terms of Service
  • Privacy Policy

Recall data is sourced from official U.S. government agencies (CPSC, FDA, NHTSA, USDA) and processed using AI to improve readability. This site is not affiliated with or endorsed by any government agency. Always refer to the original agency notice for authoritative information.

ยฉ 2026 Go Backs. All rights reserved.

Critical RiskFDA Device
Medical Devices

HeartMate Mobile Power Units Recalled for Unintended Disconnect Risk

Agency Publication Date: August 13, 2025
Share:
Sign in to monitor this recall

Summary

Thoratec LLC has recalled 657 HeartMate Mobile Power Units and AC Power Cords (Model 107754 and 107760). The recall is due to a misaligned V-Lock feature on the power cords which prevents the locking mechanism from properly engaging, potentially causing the device to lose power unexpectedly. These units are critical components of the HeartMate 2 and 3 Left Ventricular Assist Systems (LVAS), which support heart function in patients with advanced heart failure. No injuries or incidents have been reported in the provided documentation.

Risk

The misaligned locking mechanism can cause an unintended power disconnect while the heart pump is in use. If the pump loses power and stops, patients may suffer serious health complications or death from a lack of blood flow.

What You Should Do

  1. This recall affects the HeartMate Mobile Power Unit and AC Power Cord, which are components used with HeartMate 2 and HeartMate 3 Left Ventricular Assist Systems.
  2. Identify your device by checking the model numbers (107760 or 107754) and Unique Device Identifiers (UDIs) located on the product labels. See the Affected Products section below for the full list of affected codes.
  3. Stop using the recalled device immediately if you have access to a backup power source as instructed by your clinical team.
  4. Contact Thoratec LLC or your medical device distributor to arrange for a return, replacement, or correction of the power unit and power cord.
  5. Call the FDA at 1-888-463-6332 (1-888-INFO-FDA) if you have any additional questions regarding this recall.

Your Remedy Options

๐Ÿ“‹Other Action
How to: Stop using the recalled device. Contact the manufacturer or your distributor to arrange return, replacement, or correction.

Affected Products

Product: HeartMate Mobile Power Unit, AC Power Cordby HeartMate
Model / REF:
107760
UDI:
05415067038258

Refer to Attachment F for specific Lot Numbers as indicated in the recall notice.

Product: HeartMate Mobile Power Unitby HeartMate
Model / REF:
107754
UDI:
05415067038234

Refer to Attachment F for specific Serial Numbers as indicated in the recall notice.

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 97256
Status: Active
Manufacturer: Thoratec LLC
Sold By: Thoratec LLC; Hospitals; Medical Device Distributors
Manufactured In: United States
Units Affected: 2 products (53; 604)
Distributed To: Alabama, Arkansas, Arizona, California, Colorado, Connecticut, Delaware, Florida, Georgia, Iowa, Illinois, Indiana, Kansas, Kentucky, Louisiana, Massachusetts, Maryland, Maine, Michigan, Minnesota, Missouri, Mississippi, North Carolina, Nebraska, New Jersey, New Mexico, New York, Ohio, Oklahoma, Pennsylvania, South Carolina, Tennessee, Texas, Utah, Virginia, Washington, Wisconsin, West Virginia

Were You Affected by This Recall?

If you or a family member were harmed by this recalled product, you may have legal rights. Consider consulting a consumer protection attorney to understand your options for compensation.

Find an Attorney

This is general information, not legal advice. Go Backs is not a law firm and does not provide legal services.

AI-Enhanced Content: The summary, action steps, and risk assessment on this page were generated by AI from official government recall data to improve readability. This is not legal or medical advice. Always refer to the official agency sources below for authoritative information.

Sources: FDA iRES ยท Raw API Response

openFDA Disclaimer: This recall information is sourced from the openFDA API. Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. Refer to the openFDA terms of service for more information.