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FDA Medical Device Recalls (openFDA)

Thoratec LLC: 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.

Recall number
Z-1570-2025
Recalling firm
Thoratec LLC
Product
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.
Status
Open, Classified
Initiated
2025-03-13
Posted
2025-04-17
Terminated
not on file
Reason
Left Ventricular Assist System Mobile Power Unit (MPU) may have electrical component that may cause MPU not to turn on, unprompted shut down, or turning off/restarting, may cause system controller to indicate Yellow Wrench or No External Power alarms. If MPU losses power, System Controller can support the pump up to 15 minutes, and if not switched to rechargeable batteries, pump may lose power.
Root cause
Process control
Action
On 3/13/2025, recall notices were sent to customers who were asked to do the following: If patients are/ and are not able to be identified using the serial number list, send those patients the patient letter. If the MPU is not listed, this device is not affected. For units in use that have experienced MPU power issues: If there is an MPU power failure, transfer the patient from the MPU to the 14V rechargeable batteries within 15 minutes (see IFU). The Backup Battery in the System Controller will temporarily power the pump during a power source switch for up to 15 minutes. MPU will continue to echo the controller alarms as long as the internal AA batteries in the MPU do not need replacement. Do not continue to use the MPU and contact firm's Technical Support at 1-800-456-1477 (8 AM EST to 7 PM EST) for return and replacement. For units in use but not experiencing MPU power issues: Provide patient letter and educate about the issue. Ensure the patient's 14V rechargeables are ready and available for use. Prompt patient to replace AA batteries inside the MPU immediately if the Yellow Mobile Power Unit Battery Indicator alarm is active. Firm will replace these with new units starting June 2025. Return/replace units not distributed, not in use, on shelves, or that are unopened. Contact Customer Support at 1-612-444-3013, Option 2 (9 AM EST to 6:30 PM EST). Complete/return the acknowledgement form via email to MCSHMNotices@abbott.com Distribute this notice to those who need to be aware within your institution and to any organization to which these devices may have been transferred. Device lookup tool with the impacted MPU devices, available by March 24th, 2025: https://www.cardiovascular.abbott/us/en/hcp/products/heart-failure/left-ventricular-assistdevices/ heartmate-3/indications-safety-warnings/advisories.html by March 24th, 2025. If you have questions, contact Technical Support.
Quantity
1661
Distribution
Worldwide - US Nationwide distribution in the states of WA, NE, VA, PA, DC, KY, CA, IL, WI, TX, MA, AR, MS, MI, OH, FL, NC, TN, LA, NJ, UT, NY, DE, CT, GA, IN, AZ, OK, MO, OR, MN, SC, NM, MD, IA, KS, AL, CO, ME and the countries of ALGERIA, AUSTRALIA, AUSTRIA, BELGIUM, BRAZIL, CHILE, CZECH REPUBLIC, FINLAND, FRANCE, GEORGIA, GERMANY, HONG KONG, ISRAEL, ITALY, JAPAN, KUWAIT, LEBANON, LITHUANIA, NETHERLANDS, NEW ZEALAND, NORWAY, OMAN, POLAND, PORTUGAL, ROMANIA, SERBIA, SINGAPORE, SOUTH AFRICA, SOUTH KOREA, SPAIN, SWEDEN, SWITZERLAND, TAIWAN, TUNISIA, TURKEY, UK, UNITED ARAB EMIRATES.
Lot, serial or model codes
UDI-DI: 05415067038234. MPUs distributed between April 2024 and February 2025. 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510(k) numbers
not on file
PMA numbers
["P160054","P060040"]
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

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