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Recall Observatory FDA recall evidence

Device product

Arrow AutoCAT2 Intra-Aortic Balloon Pump, AC3 IABP NA/EMEA, REF IAP-0600 (IPN917287), cardiac pump

Z-0434-2023

October 17, 2022

Class I

Product summary

Firm
ARROW INTERNATIONAL Inc.
Event
Event 91021
Status
Ongoing
Classification
Class I
Quantity
N/A
Official record key
device-enforcement:Z-0434-2023

Official wording

Reason: There is a potential issue with short battery run-times on the affected intra-aortic balloon pump (IABP) devices.

Code information: UDI/DI (01) 2 0801902 17208 6, (01) 2 0801902 17208 9, All Lot/Serial Numbers

Distribution pattern: Worldwide

Derived failure modes

  • Unknown

    reason.no_named_rule · v1.0.0

    There is a potential issue with short battery run-times on the affected intra-aortic balloon pump (IABP) devices.