FDAMay 2, 2018device

Heartware Medtronic HVAD System for cardiac use. Including the following parts: (a) Controller / Controller Kits, Product numbers: 1400, 1401, 1403, 1407, 1420 (b) DC Adapter, Product numbers: 1435, 1440 (c) AC Adapter, Product numbers: 1425, 1430 (d) Battery Pack, Product number: 1650DE Indicati...

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

The hazard

Possible transient electrical connection interruption between an HVAD System power source (Battery, AC Adapter, or DC Adapter) and the Controller, while the power source is connected, that may cause unintended switching to the secondary power source and/or unexpected audible tones (beeping). The interruption typically lasts 1-2 seconds, due to oxidation between power source connector and socket.

What to do

FDA enforcement status: Ongoing

Brands named

heartware

UPCs

008887070001160088870700047500888707000291008887070007270088870700071000888707000734008887070007410088870700076500888707000758008887070007890088870700077200888707000499

Recall history

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

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