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).
Baxter Healthcare is recalling Novum IQ Syringe Pumps due to software issues that could cause the device to show a blank run screen or make false motor movements. This could lead to incorrect medication delivery if the pump malfunctions during use.
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 if the pump malfunctions during use.
Healthcare professionals and patients using the Novum IQ Syringe Pump for medical infusions are affected. Those with the specific product code and serial numbers listed in the recall are most at risk.
Check for the product code 40800BAXUS on the pump. The recall includes all units with the specific serial numbers listed in the official notice.
Look for a blank run screen or false motor movement errors on the pump display.
The product code is 40800BAXUS.
Check for the product code 40800BAXUS and the specific serial numbers listed in the recall notice.
The recall record does not mention a remedy or fix.
We’ve drafted a message you can send Baxter Healthcare to request your refund or repair — edit it as you like.
Subject: Recall Z-2333-2025 — Baxter Healthcare Baxter Healthcare Hello, I own a Baxter Healthcare that is covered by recall Z-2333-2025 from Baxter Healthcare. 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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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.
