Baxter Healthcare Corporation: Baxter Novum IQ Syringe Pump, Model Number 40800BAXUS
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The text below is copied from the official FDA (device) record. If anything differs, the official notice is correct.
- Company / brand
- Baxter Healthcare Corporation
- Product
- Baxter Novum IQ Syringe Pump, Model Number 40800BAXUS
- Reason / hazard
- 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
- Status
- Ongoing
- Distribution / sold at
- 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.
- Recall initiated
- 2026-08-11
- Code info
- UDI-DI 05413765852428, all serial numbers
- Product quantity
- 14601 units
- Voluntary mandated
- Voluntary: Firm initiated
- City
- Deerfield
- State
- IL
- Country
- United States
- Event id
- 99557
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