FDAOctober 10, 2023device

Automated Impella Controller (AIC), product number 0042-040-US with software versions V8.4 and V8.4.1.

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

The hazard

Pump not detected as connected to controller due to software issue.

What to do

FDA enforcement status: Terminated

Brands named

abiomed

UPCs

00813502011401

Recall history

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

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