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Recall Observatory FDA recall evidence

Device product

Arrow AutoCAT2 Intra-Aortic Balloon Pump, AUTOCAT2 WAVE, REF IAP-0500 (IPN000320), cardiac pump

Z-0429-2023

October 17, 2022

Class I

Product summary

Firm
ARROW INTERNATIONAL Inc.
Event
Event 91021
Status
Ongoing
Classification
Class I
Quantity
2678 units
Official record key
device-enforcement:Z-0429-2023

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) 0 0801902 05171 4, (01) 0 0801902 05171 5, 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.