Product Wiki · Recalls · U.S. FDA — Device Enforcement

Recall Z-2290-2025 — Brand Name: HeartMate Product Name: Mobile Power Unit, AC Power Cord Model/Catalog Number: 107760 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 ther

U.S. FDA — Device Enforcement · United States · 2025-06-23 · Class I

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Agency: U.S. FDA — Device Enforcement
Recall identifier: Z-2290-2025
Date of alert: 2025-06-23
Country / jurisdiction: United States
Risk level: Class I
Risk type: recall
Brand: Thoratec LLC
Product category: device
Product type: Devices
Barcode (EAN/GTIN): 05415067038258

Reported risk: Due to misaligned V-Lock feature on the Mobile Power Unit power cords, which prevents the locking mechanism from properly engaging with the Mobile Power Unit and may cause unintended disconnect.

Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

Verify each fact at the issuing agency before acting. Recall scope, affected lots, and remediation instructions may be updated by the agency after our last sync.

ProductGuru indexes recall and safety-alert records from ~30 public agency registries. We are not lawyers, regulators or product-safety consultants. This page restates what the named agency published; consult the primary source above (or qualified counsel in your jurisdiction) before any commercial, medical or safety decision.

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