Data Foundry

Medical device recalls 2026

Brand Name: HeartMate Product Name: HeartMate 3 Left Ventricular… — Class II medical device recall Z-2518-2026

Ongoing recall by Thoratec LLC, reported 2026-06-24, distributed nationwide. Due to 11 volt Backup Battery failures.

Recall numberZ-2518-2026
Product typeMedical device
ClassificationClass II
StatusOngoing
Voluntary or mandatedVoluntary
Recalling firmThoratec LLC, Pleasanton, CA, United States
Recall initiated2026-05-13
Classified2026-06-18
Reported by FDA2026-06-24
DistributedNationwide (US)
Countries outside the USCA, DE, ES, JP, NL, PL
Quantity4
UPC / GTIN / UDI-DI05415067039323
Model numbers106524US

Product

Brand Name: HeartMate Product Name: HeartMate 3 Left Ventricular System (LVAS) Kits Model/Catalog Number: 106524US Software Version: N/A Product Description: The HeartMate 3" Left Ventricular Assist System (LVAS) is a set of equipment and materials that together comprise a medical device designed to provide therapeutic benefit to those affected with advanced heart failure. In service, the LVAS assumes some or all of the workload of the left ventricle, thereby restoring the patient's systemic perfusion while palliating the underlying pathology. The LVAS features a Left Ventricular Assist Device (LVAD), a blood pump intended for long-term implantation in such patients, an extracorporeal Controller, plus all of the features, controls, attachments, interfaces, power sources, supporting equipment, labeling, and tools required to achieve the desired therapeutic benefit. Component: No

Reason for recall

Due to 11 volt Backup Battery failures.

Machine access

This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-2518-2026. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.

Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.