Thoratec Corp. 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, REF 106524US, UDI or GTIN: 00813024013297, and 106524, UDI or GTIN: 00813024011712 - Product Usage: Provides power to the System Controller and pump. - Provides power to the System Monitor when it is connected to the Power Module. - Connects the System Monitor to the System Controller for monitoring purposes. - Echoes S Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
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, REF 106524US, UDI or GTIN: 00813024013297, and 106524, UDI or GTIN: 00813024011712 - Product Usage: Provides power to the System Controller and pump. - Provides power to the System Monitor when it is connected to the Power Module. - Connects the System Monitor to the System Controller for monitoring purposes. - Echoes S
Brand
Thoratec Corp.
Lot Codes / Batch Numbers
All serial numbers.
Products Sold
All serial numbers.
Thoratec Corp. is recalling HeartMate 3 Mobile Power Unit, REF 107754, UDI or GTIN: 00813024010883, and 107758, UDI or GTIN: 008 due to Excessive static electricity can potentially cause unrecoverable power loss and damage to the mobile power unit that can be used to power the left ven. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Excessive static electricity can potentially cause unrecoverable power loss and damage to the mobile power unit that can be used to power the left ventricular assist system, which could lead to no or reduced blood flow from the left ventricular assist system.
Recommended Action
Per FDA guidance
On 12/02/19, Urgent Medical Device Recall notices were delivered in person by field representatives who provided training on the methods to reduce generation of excessive static electricity. Clinician were advised the following: Recognition of alarms if the Left Ventricular Assist System (LVAS), when connected to the MPU Module, has been impacted by excessive static electricity. " If a patient is not sleeping or resting, battery power is recommended instead of the MPU Module to power the LVAS in order to reduce the impact of static electricity. " In any case of an unexpected "no external power" alarm, patients should connect to battery power to the LVAS before attempting to determine the cause of the alarm. If the alarm persists, the patient should call the Hospital Contact. " To prevent the generation of excessive static electricity during daily activities, the firm is providing clarification for static electricity management when using the MPU Module with the LVAS. Refer to Appendix A for specific reminders and recommendations to prevent excessive static electricity. Contact all patients with affected devices as soon as possible and provide them with the information in Appendix A. Also, please complete the attached acknowledgement form. Clarifications will be added to the Instructions for Use and Patient Handbook in the future. Customers with additional questions are encouraged to call 1-800-456-1477 or to contact their field representative. Using battery power will help avoid system damage from static electricity. If you're on the MPU, switch to battery power when doing things that cause static electricity. Reduce static electricity, with products such as: 1) A humidifier to add moisture to the air, 2) Dryer sheets and fabric softeners to reduce the buildup of static electricity in clothes and bedsheets, 3) Anti-static spray on carpets and other materials to reduce the buildup of static electricity 4) Skin moisturizers to make your skin less
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticePage updated: Jan 10, 2026