Arrow AutoCAT2 IABP Pump: Short Battery Run Times Risk

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Recalling firmARROW INTERNATIONAL Inc.3015 Carrington Mill Blvd, N/A · Morrisville, NC 27560-5437

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✎ GovInfoNow plain-language explainer

What happened, in plain English

Arrow is recalling certain AutoCAT2 Intra-Aortic Balloon Pumps due to potential short battery run times. This could lead to device failure during use, which is critical for patients requiring heart support.

Why it’s dangerous

The pumps may run out of battery faster than expected, potentially causing device failure during critical medical procedures. This could lead to interruption of heart support for patients.

Who’s affected

Patients using the recalled cardiac pumps are most at risk. The affected units are typically used in hospitals for heart support.

How to tell if you have this one

Check for the model AC3 IABP NA/AJLA with reference number IAP-0601(IPN916548). The units were sold with specific lot/serial numbers listed in the recall notice.

Brand
Arrow
Category
Medical device

Based on the official FDA remedy

What to do — step by step

Check Device Details
Verify the model number and reference code on your pump to confirm if it's affected.

✎ GovInfoNow

Questions people ask

Is this pump dangerous?

The recall states there is a potential issue with short battery run times, which could lead to device failure. However, the hazard is not described as causing serious injury in normal use.

How do I know if my pump is affected?

Check for the model AC3 IABP NA/AJLA with reference number IAP-0601(IPN916548) and specific lot/serial numbers listed in the recall notice.

What should I do if my pump is affected?

The recall does not specify a remedy, so contact Arrow International for further instructions.

Take action

Contact Arrow

We’ve drafted a message you can send Arrow to request your refund or repair — edit it as you like.

✉️ Open in email

Subject: Recall Z-0436-2023 — Arrow Arrow

Hello,

I own a Arrow that is covered by recall Z-0436-2023 from Arrow.

I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this?

Thank you.

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Where this comes from

The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.

Official source: FDA Recall #Z-0436-2023 (October 17, 2022) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-0436-2023 to see it in context.
Plain-language summary written by qwen3:4b on August 19, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.

ARROW INTERNATIONAL Inc. recalls Arrow AutoCAT2 Intra-Aortic Balloon Pump, AC3 IABP NA/AJLA, REF IAP-0601(IPN916548), cardiac pump

Lower-risk recall