Baxter Novum IQ LVP Infusion Pump Recall: Software Errors May Cause Blank Screen

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Contact the company & request your remedy

Recalling firmBaxter Healthcare Corporation1 Baxter Pkwy, N/A · Deerfield, IL 60015-4625

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

✎ GovInfoNow plain-language explainer

What happened, in plain English

Baxter is recalling Novum IQ Large Volume Pumps because software problems might cause the pump to show a blank screen or move incorrectly. This could lead to incorrect medication delivery during IV treatments.

Why it’s dangerous

The software anomalies may cause the pump to display a blank run screen or trigger false motor movements. This could result in incorrect medication delivery during IV treatments.

Who’s affected

Patients using the Novum IQ LVP or SP pumps for IV treatments are affected. Healthcare providers and patients receiving IV therapy are most at risk.

How to tell if you have this one

Check for the product code 40700BAXUS on the pump. The pump has a unique identifier (UDI/DI) starting with 05413765851797. All serial numbers are affected.

Brand
Baxter
Category
Medical device

Based on the official FDA remedy

What to do — step by step

Check Pump Status
Look for a blank run screen or false motor movement errors on the pump display.

✎ GovInfoNow

Questions people ask

What is the product code for the recalled pumps?

The product code is 40700BAXUS.

What should I do if I see a blank screen?

If you see a blank run screen, stop using the pump immediately and contact Baxter for assistance.

Is there a fix for this issue?

The recall record does not mention a specific fix or remedy.

Take action

Contact Baxter

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

✉️ Open in email

Subject: Recall Z-2332-2025 — Baxter Baxter

Hello,

I own a Baxter that is covered by recall Z-2332-2025 from Baxter.

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-2332-2025 (August 4, 2025) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-2332-2025 to see it in context.
Plain-language summary written by qwen3:4b on August 17, 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.

Baxter Healthcare Corporation recalls Novum IQ LVP (Large Volume Pump), Product Code 40700BAXUS, infusion pump

Use caution until it’s fixed