Serious health hazard — there is a reasonable probability that use of or exposure to this product will cause serious adverse health consequences or death.
Arrow AutoCAT 2 Intra-Aortic Balloon Pump Recalled by ARROW INTERNATIONAL Inc. Due to There is a potential issue with short battery...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact ARROW INTERNATIONAL Inc. directly.
Affected Products
Arrow AutoCAT 2 Intra-Aortic Balloon Pump, Arrow AutoCAT 2 IABP, REF IAP-0400F (IPN000306), cardiac pump
Quantity: 1 unit
Why Was This Recalled?
There is a potential issue with short battery run-times on the affected intra-aortic balloon pump (IABP) devices.
Where Was This Sold?
Worldwide
About ARROW INTERNATIONAL Inc.
ARROW INTERNATIONAL Inc. has 47 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report