Baxter recalls Novum IQ Syringe Pump model 4080: software issue may cause infusion errors if syringe reaches empty during multi-syringe infusions. Affected units have specific serial numbers and model numbers.
A software issue that may occur during a Volume/Time (VOT) multi-syringe infusion when a syringe reaches empty and is replaced while a Volume To Be Infused (VTBI) remains.
Baxter is recalling its Novum IQ Syringe Pump model 40800BAXUS due to a software issue that could cause infusion errors when replacing a syringe that has reached empty during multi-syringe treatments. This affects patients using the pump for medical infusions and requires attention to prevent potential treatment errors.
The software issue can cause the pump to continue infusing medication after a syringe is empty, potentially leading to incorrect dosing if a new syringe is replaced during the infusion process. This may result in treatment errors for patients receiving multi-syringe infusions.
Patients using the Baxter Novum IQ Syringe Pump model 40800BAXUS for medical infusions are most at risk. Healthcare providers and patients who have purchased or received this pump are affected.
Check for the model number 40800BAXUS on the pump. Affected units also have specific serial numbers and UDI-DI 05413765852428 as listed in the recall notice.
Look for the model number 40800BAXUS on the syringe pump to confirm if it is affected.
The recall indicates a potential software issue that could cause infusion errors, so it is recommended to check if your pump is affected before use.
Check for the model number 40800BAXUS and the specific serial numbers listed in the recall notice.
The recall does not specify a remedy, so affected users should check with Baxter Healthcare Corporation for further instructions.
We’ve drafted a message you can send Baxter to request your refund or repair — edit it as you like.
Subject: Recall Z-3065-2026 — Baxter Baxter Hello, I own a Baxter that is covered by recall Z-3065-2026 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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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.
