Baxter recalls NovumIQ syringe pumps with serial numbers starting 02A220600103 due to an incorrectly installed gasket that could allow fluid to enter the pump during cleaning or IV spills.
Baxter Healthcare Corporation is issuing an Urgent Medical Device Recall for the Novum IQ syringe pumps listed below due to an incorrectly installed gasket. A gasket failure could lead to potential fluid ingress due to cleaning, or as a result of an IV fluid spill.
Baxter is recalling specific NovumIQ syringe pumps because a faulty gasket might let IV fluid leak during cleaning or spills. This could lead to contamination or incorrect dosing if the pump isn't working properly.
The syringe pump has an incorrectly installed gasket that could allow IV fluid to enter the pump during cleaning or if there's a spill. This might cause contamination or incorrect medication dosing if the pump malfunctions.
Patients using Baxter NovumIQ syringe pumps with the listed serial numbers are affected. Healthcare providers and patients who use these pumps for IV therapy are at risk if the gasket fails.
Check the serial number on the pump, which starts with '02A220600103' or similar numbers listed in the recall notice. The product is identified by the UDI/DI code 05413765852428.
Look for the serial number on the pump, which starts with '02A220600103' or other numbers listed in the recall notice.
Reach out to Baxter Healthcare Corporation directly for assistance with the recall.
Baxter is recalling these pumps because an incorrectly installed gasket could allow IV fluid to enter the pump during cleaning or spills, potentially causing contamination or incorrect dosing.
Check the serial number on the pump; affected units start with '02A220600103' or other numbers listed in the recall notice.
Contact Baxter Healthcare Corporation directly for assistance with the recall.
We’ve drafted a message you can send Baxter to request your refund or repair — edit it as you like.
Subject: Recall Z-1423-2025 — Baxter Baxter Hello, I own a Baxter that is covered by recall Z-1423-2025 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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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.
