Baxter Healthcare Corporation recalls Baxter Novum IQ Syringe Pump
- Recalling company
- Baxter Healthcare Corporation
- Product
- Baxter Novum IQ Syringe Pump, Model Number 40800BAXUS
- Reason
- 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.
- Classification
- Class II – may cause temporary or medically reversible health consequences
- Recall date
- Aug 11, 2026
- Reported
- Sep 9, 2026
- Distribution
- US Nationwide distribution including in the states of AK, AL, AR, AZ, CA, CO, FL, GA, HI, IA, ID, IL, IN, KS, KY, LA, MA, MD, MI, MN, MO, MS, MT, NC, ND, NE, NH, NJ, NM, NV, NY, OH, OK, OR, PA, SC, SD, TN, TX, UT, VA, VT, WA, WI, and WV.
- Status
- Ongoing
- Quantity
- 14601 units
- Lot / codes
- UDI-DI 05413765852428, all serial numbers
- Company location
- Deerfield, IL
- Recall type
- Voluntary: Firm initiated
- Recall number
- Z-3065-2026
- Agency
- U.S. Food and Drug Administration (FDA)
View official FDA notice ↗ Search recall number Z-3065-2026 in the FDA Enforcement Report. Also see FDA recall press releases.
If you use this product, check the lot, NDC or model number against the official notice and follow its instructions. Do not stop a prescribed medicine or remove a medical device without talking to your doctor or pharmacist. Report problems to FDA MedWatch. FoodRecallNow summarizes public FDA data and is not medical advice.