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Recall Observatory FDA recall evidence

Device product

Automated Impella Controller (AIC), product number 0042-000-US with software versions V8.4 and V8.4.1.

Z-0440-2024

October 10, 2023

Class II

Product summary

Firm
Abiomed, Inc.
Event
Event 93406
Status
Terminated
Classification
Class II
Quantity
Unavailable
Official record key
device-enforcement:Z-0440-2024

Official wording

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

Code information: UDI-DI (GTIN): 00813502010022, serial numbers IC3772, IC3773, IC5721 and IC4404.

Distribution pattern: US: AZ, CA, FL, NY & VA.

Derived failure modes

  • Device software or design

    reason.device_software_design · v1.0.0

    software issue