Baxter recalls Novum IQ Syringe Pump model 40800BAXUSL due to software issue that may cause infusion errors when syringes are replaced during multi-syringe infusions. Affected units have specific serial 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 40800BAXUSL because a software issue can cause infusion errors when syringes are replaced during multi-syringe infusions. This could lead to incorrect medication dosing if not addressed.
The software issue occurs when a syringe reaches empty and is replaced while a remaining volume to be infused (VTBI) is still active. This can cause the pump to miscalculate the remaining medication volume, potentially leading to incorrect dosing during multi-syringe infusions.
Healthcare professionals using Baxter Novum IQ Syringe Pump model 40800BAXUSL for medical infusions are most at risk if they encounter the described software issue during multi-syringe treatments.
Check for the model number 40800BAXUSL on the pump. Affected units have specific serial numbers listed in the recall notice.
Look for the serial number on the pump to confirm if it is affected by this recall.
The recall specifically affects Baxter Novum IQ Syringe Pump model 40800BAXUSL with specific serial numbers. Check your pump's serial number to see if it is included.
The recall does not include a remedy or action for affected units. Check the serial number to confirm if your pump is affected.
The recall does not provide a remedy, so there is no specific action to take. However, the software issue may cause infusion errors, so it is recommended to check with Baxter if you have concerns.
We’ve drafted a message you can send Baxter to request your refund or repair — edit it as you like.
Subject: Recall Z-3066-2026 — Baxter Baxter Hello, I own a Baxter that is covered by recall Z-3066-2026 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.
