Baxter Novum IQ LVP Infusion System Recall: Underinfusion Risk

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Contact the company & request your remedy

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

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✎ GovInfoNow plain-language explainer

What happened, in plain English

Baxter is recalling its Novum IQ LVP Infusion System (REF 40700BAXUS) because it may cause underinfusion if the device is in standby mode or powered off with the infusion set still loaded. This could lead to insufficient medication delivery during critical medical treatments.

Why it’s dangerous

The device may underinfuse medication if the standby mode feature is activated or if the system is powered off while the infusion set remains loaded. This could result in insufficient medication delivery during critical medical procedures.

Who’s affected

Healthcare providers using the Baxter Novum IQ LVP Infusion System for medical treatments are most at risk. Patients receiving infusion therapy through this system could be affected if the device malfunctions.

How to tell if you have this one

Check for the Baxter Novum IQ LVP Infusion System with reference number 40700BAXUS. All units are affected regardless of serial number.

Brand
Baxter
Category
Medical device

Based on the official FDA remedy

What to do — step by step

Check Device Status
Ensure the device is not in standby mode and remains powered on when the infusion set is loaded.

✎ GovInfoNow

Questions people ask

Is this recall affecting all units?

Yes, all units of the Baxter Novum IQ LVP Infusion System (REF 40700BAXUS) are affected.

What should I do if I have this device?

Check if the device is in standby mode or powered off with the set loaded. If so, stop using it and contact Baxter for guidance.

How can I verify if my device is recalled?

Look for the reference number 40700BAXUS on the device. All units are affected.

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-1767-2025 — Baxter Baxter

Hello,

I own a Baxter that is covered by recall Z-1767-2025 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-1767-2025 (April 24, 2025) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-1767-2025 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.

Baxter Healthcare Corporation recalls Baxter Novum IQ LVP INFUSION SYSTEM, REF 40700BAXUS

Use caution until it’s fixed