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Recall Observatory FDA recall evidence

Device product

Automated Impella Controller (AIC), Product No. 0042-0000-US, 0042-0010-US, 0042-0040-US. Used with Impella Ventricular Support Systems (cardiovascular)

Z-1175-2024

March 01, 2021

Class II

Product summary

Firm
Abiomed, Inc.
Event
Event 93876
Status
Terminated
Classification
Class II
Quantity
4,463 (US)
Official record key
device-enforcement:Z-1175-2024

Official wording

Reason: Retrospective reporting for the release of Technical Bulletin IMP-2643 AIC Version 8.5 Software Update Available. The update resolved an issue in version 8.4 where a pump was not recognized by the AIC.

Code information: Product Code 0042-0000-US UDI-DI 00813502010022; Product Code 0042-0010-US UDI-DI 00813502010985; Product Code 0042-0040-US UDI-DI 00813502011401; Software Versions V8.4 and V8.4.1

Distribution pattern: US Nationwide distribution.

Derived failure modes

  • Device software or design

    reason.device_software_design · v1.0.0

    Software Update Available. The update resolved an issue