ARROW INTERNATIONAL Inc. recalls Arrow AutoCAT2 Intra-Aortic Balloon Pump, AUTOCAT2 WAVE, REF IAP-0500 (IPN000320), cardiac pump

Recalled December 21, 2022 · FDA recall Z-0429-2023 · ARROW INTERNATIONAL

Hazard

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

Units

2678 units

Sold at

Worldwide

Description

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

Product

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

Manufacturer(s)

ARROW INTERNATIONAL Inc.

Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →