Arrow AutoCAT2 Cardiac Pump Recall: Short Battery Run Times

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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 device failure during use, which is critical for patients needing heart support.

Why it’s dangerous

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

Who’s affected

Patients using the recalled cardiac pumps are most at risk. The affected units are typically used in hospitals for critical care situations.

How to tell if you have this one

Check for the model name 'AutoCAT2' or 'AUTOCAT2 WAVE', and the specific serial numbers listed in the recall notice. The affected units have the UDI/DI codes starting with (01) 0 0801902 05171.

Brand
Arrow
Category
Medical device

Based on the official FDA remedy

What to do — step by step

Check Device Serial Number
Look for the UDI/DI code starting with (01) 0 0801902 05171 on the pump's label.

✎ GovInfoNow

Questions people ask

What is the specific model of pump being recalled?

The recalled models are Arrow AutoCAT2 Intra-Aortic Balloon Pump, AUTOCAT2 WAVE, REF IAP-0500 (IPN000320).

How can I tell if my pump is affected?

Check for the UDI/DI code starting with (01) 0 0801902 05171 on the pump's label.

What should I do if I have the affected pump?

The recall does not specify a remedy, so contact Arrow International directly for guidance.

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-0429-2023 — Arrow Arrow

Hello,

I own a Arrow that is covered by recall Z-0429-2023 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-0429-2023 (October 17, 2022) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-0429-2023 to see it in context.
Plain-language summary written by qwen3:4b on August 18, 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, AUTOCAT2 WAVE, REF IAP-0500 (IPN000320), cardiac pump

Lower-risk recall