FDAJanuary 17, 2011device

Automated Impella Controller (AIC) with the below product descriptions and corresponding Product Codes. 1. Impella Controller, Packaged, CA; Product Code: 0042-0000-CA. 2. Impella Controller, Packaged, EU; Product Code: 0042-0000-EU. 3. Impella Controller, Packaged, UK; Product Code: 0042-0000-UK...

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

The hazard

Retrospective submission for following issues identified: 1. Alarm failures, power-path faults, electrical-short risks, and inaccurate motor-current sensing were identified in certain AIC consoles. 2. There is improper alignment between the purge cassette and the motor drive in the AIC. This can result in a piston block event and lead to the inability to complete priming of the purge system, requiring the user to switch to backup AIC console.

What to do

FDA enforcement status: Ongoing

Brands named

abiomed

UPCs

00813502011272008135020112890081350201129600813502010022

Recall history

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

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