Use cautionMedical device recall · FDA · Published August 4, 2025
Baxter Novum IQ Syringe Pump Recall: Software Issues May Cause Blank Screen
Baxter Healthcare recalls Novum IQ Syringe Pumps with software anomalies that may cause blank run screens or false motor errors. Affected units include Product Code 40800BAXUS with specific serial numbers.
Baxter Healthcare Corporation is issuing an Urgent Medical Device Correction for the Novum IQ Large Volume Pump (LVP) and Novum IQ Syringe Pump (SP) due to software anomalies that may result in a blank Run screen (LVP and SP) and/or false motor movement system error (SP only).
Take action
Contact the company
📍Recalling firmBaxter Healthcare Corporation1 Baxter Pkwy · Deerfield, IL 60015-4625
“Baxter Novum IQ Syringe Pump Recall: Software Issues May Cause Blank Screen.” GovInfoNow, updated August 17, 2026. https://govinfonow.com/recall/51697-baxter-novum-iq-syringe-pump-recall-software-issues-may-cause. Based on FDA recall #Z-2333-2025 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2333-2025%22&limit=1).
Baxter Healthcare Corporation recalled Novum IQ Syringe Pump, Product Code 40800BAXUS, due to software anomalies causing blank screens or false motor errors, according to the FDA on Aug. 4, 2025. Owners should contact Baxter for a remedy.
How to tell if you have it
Brand: Baxter Healthcare
Product: Novum IQ Syringe Pump
Product Code: 40800BAXUS
Product: Novum IQ Large Volume Pump (LVP)
Product: Novum IQ Syringe Pump (SP)
UDI/DI: 05413765852428
Serial Numbers: All Serial Numbers
The hazard
The recall involves software anomalies that may result in a blank Run screen for both the Large Volume Pump and Syringe Pump, and/or a false motor movement system error for the Syringe Pump only. The FDA classified this as an Urgent Medical Device Correction.
Context
GovInfoNow's records show Baxter Healthcare Corporation has 187 other recalls on record since Sept. 2, 2015. Other recent recalls of similar products include Baxter PRO+ 40" MRS SURFACE Mattress Recall (Aug. 18, 2026), Baxter 0.9% Sodium Chloride Injection Recall (Aug. 17, 2026), and Baxter Dextrose 2000mL Bags Recall (Aug. 17, 2026). Other recent recalls of similar products include Fresenius Kabi Ivenix Infusion System Software Recall (May 6, 2026) and Medtronic MiniMed 780G Insulin Pump Recall (May 27, 2026).
How to tell if you have this one
Check for the product code 40800BAXUS on the pump. The recall includes all units with the specific serial numbers listed in the official notice.
Brand
Baxter Healthcare
Category
Medical device
FDA recall event · 3 products
All 3 products in this recall
FDA lists each product line separately under one recall event. Check your product description, lot or code numbers against each row. Every row shares the hazard and remedy on this page.
Classification
Class I
Status
Ongoing
Distribution
US distribution including Puerto Rico and OUS (International) Canada
Recall number
Product, codes & lots
Quantity
Z-2332-2025
Novum IQ LVP (Large Volume Pump), Product Code 40700BAXUS, infusion pump; UDI/DI 05413765851797, All Serial Numbers
43,922 units
Z-2333-2025
Novum IQ Syringe Pump, Product Code 40800BAXUS, infusion pump; UDI/DI 05413765852428, All Serial Numbers
10,101 units
Z-2334-2025
Novum IQ Syringe Pump, Product Code 40700BAX, infusion pump; UDI/DI N/A, All Serial Numbers
22703 units
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.
Where it went and when
Where it was distributed
Distributed nationwide, and outside the U.S.
Nationwide
Not listed
FDA distribution: “US distribution including Puerto Rico and OUS (International) Canada” States read from FDA’s own wording; “not listed” means the notice does not name it.
Distributed nationwide, and outside the U.S.
Recall timeline
FDA published this recall 37 days after the firm started it.
1Firm started the recall
2FDA classified it Class I
3Published in FDA’s Enforcement Report
Dates from the agency record only; steps without a date are left out.
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-2333-2025 (August 4, 2025) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-2333-2025 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.