Official recall notice

FDA DeviceClass IINotable

FDA Recall: Brand Name: HeartMate Product Name: HeartMate 3 Left Ventricular System (LVAS) Kits Model/Catalog

Recall date
2026-06-24
FDA class
Class II

Why it was recalled

Hazard

Due to 11 volt Backup Battery failures.

Recommended action

What to do

4

Product description

Due to 11 volt Backup Battery failures.

Related Recalls