Arrow AutoCAT2 IABP Pump: 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 AutoCAT2 intra-aortic balloon pumps due to potential short battery run times. This could lead to the pump failing during use, which is critical for patients needing heart support.

Why it’s dangerous

The pumps may run out of battery faster than expected, potentially stopping support for patients with heart conditions. This could cause serious complications if the pump fails during critical medical procedures.

Who’s affected

Patients using the recalled pumps for cardiac support are most at risk. The affected units are identified by specific serial numbers and lot codes.

How to tell if you have this one

Check the serial numbers on the pump: (01) 2 0801902 17208 6 or (01) 2 0801902 17208 9. The product was sold with specific lot codes and serial numbers as listed in the recall notice.

Brand
Arrow
Category
Medical device

Based on the official FDA remedy

What to do — step by step

Check Serial Numbers
Look for the serial numbers (01) 2 0801902 17208 6 or (01) 2 0801902 17208 9 on the pump.

✎ GovInfoNow

Questions people ask

Why is this pump being recalled?

The recall is due to potential short battery run times, which could cause the pump to fail during critical medical use.

How do I know if my pump is affected?

Check the serial numbers: (01) 2 0801902 17208 6 or (01) 2 0801902 17208 9.

What should I do if I have the affected pump?

Contact Arrow directly for further instructions on the recall.

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-0434-2023 — Arrow Arrow

Hello,

I own a Arrow that is covered by recall Z-0434-2023 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-0434-2023 (October 17, 2022) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-0434-2023 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/EMEA, REF IAP-0600 (IPN917287), cardiac pump

Use caution until it’s fixed