FDA Medical Device Recalls (openFDA)
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 System Controller alarms. The Mobile Power Unit is for home or clinical use when the patient does not require monitoring using the System Monitor. The Mobile Power Unit is used when the patient is indoors, stationary, or sleeping. The System Controller and the Mobile Power Unit are connected through the Mobile Power Unit patient cable. The cable transfers power from the Mobile Power Unit to the System Controller.
- Recall number
- Z-0746-2020
- Recalling firm
- Thoratec Corp.
- 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 System Controller alarms. The Mobile Power Unit is for home or clinical use when the patient does not require monitoring using the System Monitor. The Mobile Power Unit is used when the patient is indoors, stationary, or sleeping. The System Controller and the Mobile Power Unit are connected through the Mobile Power Unit patient cable. The cable transfers power from the Mobile Power Unit to the System Controller.
- Status
- Terminated
- Initiated
- 2019-12-02
- Posted
- not on file
- Terminated
- 2022-09-14
- Reason
- 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.
- Root cause
- Device Design
- Action
- 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
- Quantity
- 13871
- Distribution
- US Nationwide distribution in the states of MN, PA, IL, NJ, WI, AZ, AR, TN, MO, TX, MA, NE, MI, CA, NC, CO, OH, DE, FL, NY, IN, GA, VA, DC, CT, OK, UT, KY, MD, OR, NM, ME, SC, IA, WA, LA, NV, AL, KS, MS, WV.
- Lot, serial or model codes
- All serial numbers.
- 510(k) numbers
- not on file
- PMA numbers
- ["P160054"]
- Product code
- DSQ
- Firm FEI
- 2916596
- Firm city
- Pleasanton
- Firm state
- CA
- Firm country
- not on file
Where this comes from
- Register
- FDA Medical Device Recalls (openFDA)
- Publisher
- U.S. Food and Drug Administration (openFDA)
- File
- device-recall-0001-of-0001.json.zip
- sha256
- b87518bfe2e8
- Size
- 288210821 bytes
- Published
- 2026-09-28
- Read
- 2026-09-29T08:25:23.626Z
- Source file
- Source file retained · verify
- Refresh due
- 2026-10-06
Unless otherwise noted, the content, data, documentation, code, and related materials on openFDA is public domain and made available with a Creative Commons CC0 1.0 Universal dedication.
Cite as
FDA Medical Device Recalls (openFDA) (U.S. Food and Drug Administration (openFDA)), device-recall-0001-of-0001.json.zip, sha256 b87518bfe2e8, published 2026-09-28