Official recall record
Impella® Controller (ref 77714)
- Issuing authority
- Health Canada — Medical Devices
- Published
- 2025-07-09
- Country of alert
- Canada
- Alert level
- Type I
- Alert type
- recall
What the authority reported
Abiomed has identified an Automated Impella Controller™ (AIC) issue that may impair the detection of an Impella® pump when connected to an AIC. The pump detection issue may occur with any of the Abiomed Impella® pumps and may occur during console-to-console transfer or case start. There is no visual alarm displayed on the AIC screen to indicate the detection issue in these situations. Recall start date: July 7, 2025
What to do
Follow the instructions in the official notice — recall remedies (refund, repair, replacement, or disposal) are defined by the issuing authority and the responsible business, and they differ per recall. Do not rely on summaries, including this one.
Verify at the source:
Health Canada — Medical Devices — official record →
Record last checked against the registry on 2026-05-31.
Record last checked against the registry on 2026-05-31.
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