Regulator FDA — Thoratec LLC device-recallcardiac-rehabpatient-safety

FDA recall: Brand Name: HeartMate

FDA — Thoratec LLC · 2025-06-23 · By Thoratec LLC

The FDA has classified an open recall for Thoratec's HeartMate 3 Left Ventricular Assist System Mobile Power Unit AC Power Cord (Model 107760). A manufacturing defect causes the V-Lock feature on the power cord to be misaligned, preventing the locking mechanism from fully engaging and creating a risk of unexpected disconnection. Physical therapists working with patients who have LVADs should be aware of this power supply safety issue during mobility and rehabilitation sessions.

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