Arrow AutoCAT2 IABP Pumps: Short Battery Run Times Risk

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Contact the company & request your remedy

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

No email on file — write to the address above instead.

✎ GovInfoNow plain-language explainer

What happened, in plain English

Arrow is recalling certain AutoCAT2 Intra-Aortic Balloon Pumps because they may have short battery run times. This could lead to the pump failing during use, which is dangerous for patients needing heart support.

Why it’s dangerous

The pumps may run out of battery faster than expected, potentially causing the device to stop working during critical medical procedures. This could lead to complications for patients with heart conditions who rely on the pump for support.

Who’s affected

Patients using the recalled pumps for heart support are most at risk. Healthcare providers who use these pumps in medical settings may also be affected.

How to tell if you have this one

Check for the model AC3 IABP NA/AJLA with reference number IAP-0601(IPN917:288). The product has 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 Battery Status
Verify if the pump has short battery run times by testing the device's battery life.
Contact Manufacturer
Reach out to Arrow International for guidance on whether the pump needs replacement.

✎ GovInfoNow

Questions people ask

Do I need to stop using this pump immediately?

The recall does not require immediate stoppage; however, users should check battery status and contact Arrow if concerns arise.

What should I do if my pump has short battery life?

Contact Arrow International for assistance with potential replacement or repair.

How can I confirm if my pump is affected?

Check the model AC3 IABP NA/AJLA with reference number IAP-0601(IPN917288) and specific lot/serial numbers listed in the recall notice.

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-0437-2023 — Arrow Arrow

Hello,

I own a Arrow that is covered by recall Z-0437-2023 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-0437-2023 (October 17, 2022) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-0437-2023 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(IPN917288), cardiac pump

Use caution until it’s fixed