# FDA device recall: Automated Impella Controller (AIC), for use with left heart support blood pump.  Labeled as the following with correspon

> recall · VERIFIED · 2026-05-14

Firm: Abiomed, Inc. · Class I · Potential software error in the Automated Impella Controller ("AIC" ) when used in conjunction with left ventricular Impella devices.

- Company: Abiomed, Inc.
- Sector: medtech
- Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

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Source: MedFuel Intel news monitor. Verification tier: VERIFIED. Informational only, not investment advice. Corrections: media@medfuelinc.com.