FDAFebruary 19, 2024device

HeartMate 3 Left Ventricular Assist System (LVAS): 1. HeartMate 3 Sealed Outflow Graft with Bend Relief, Investigational Device Exemption (IDE) 2. HeartMate 3 Sealed Outflow Graft with Bend Relief, US 3. HeartMate 3 Sealed Outflow Graft with Bend Relief, OUS 4. HeartMate 3 LVAS Implant Kit, IDE 5...

Official recall recorded by the U.S. Food & Drug Administration.

The hazard

Observed outflow graft deformation known as Extrinsic Outflow Graft Obstruction (EOGO) associated with Left Ventricular Assist System.

What to do

FDA enforcement status: Ongoing

Brands named

thoratec

UPCs

00813024013266008130240116750081302401329700813024011712

Recall history

Other federal recalls tied to the same brand — a factual pattern, straight from the source data.

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