Arrow AC3 Optimus IABP: Short Battery Run Times Risk

Take action

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 intra-aortic balloon pumps that may run out of battery too quickly. This could cause the pump to stop working during critical cardiac support, risking serious health consequences.

Why it’s dangerous

The pumps may run out of battery faster than expected, which could stop the pump from supporting the heart. This might happen during critical medical procedures or when the patient is unstable.

Who’s affected

Patients using the Arrow AC3 Optimus IABP pumps for cardiac 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 number AC3 Optimus IABP NA/AJLA, reference number IAP-0701 (IPN917286), or lot/serial numbers listed in the recall notice. The product is used in cardiac care settings.

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 life by monitoring usage during cardiac support sessions.
Contact Manufacturer
Reach out to Arrow International for specific guidance on whether your pump needs replacement.

✎ GovInfoNow

Questions people ask

Why is this pump being recalled?

The recall is due to potential short battery run-times that could cause the pump to stop working during critical cardiac support.

Do I need to stop using this pump immediately?

No, but you should check battery status and contact Arrow International for specific guidance.

How can I tell if my pump is affected?

Check for the model number AC3 Optimus IABP NA/AJLA, reference number IAP-0701 (IPN917286), or 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-0443-2023 — Arrow Arrow

Hello,

I own a Arrow that is covered by recall Z-0443-2023 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.

Similar recalls

From people who’ve dealt with this

Experiences, tips, and questions from readers. Every comment is reviewed before it appears.

No comments yet — be the first to share your experience.

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-0443-2023 (October 17, 2022) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-0443-2023 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 AC3 Optimus Intra-Aortic Balloon Pump, AC3 Optimus IABP NA/AJLA, REF IAP-0701 (IPN917286), cardiac pump

Use caution until it’s fixed