Baxter Healthcare Corporation — Baxter Novum IQ Syringe Pump, Model Number 40800BAXUS
Official product recall notices and clearly labeled enforcement reference records.
Reference record — not a live warning · enforcement-reference · official-source
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.
- Provider
- FDA — device enforcement reference
- Source observed
- 8/11/2026, 12:00:00 AM UTC
- Source updated
- 8/31/2026, 12:00:00 AM UTC
- Location
- Deerfield, IL, US
- 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.
- notice
- Periodic enforcement reference; not a real-time safety alert or a reliable recall-lifecycle tracker.
- product
- Baxter Novum IQ Syringe Pump, Model Number 40800BAXUS
- 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.
- event number
- 99557
- manufacturer
- Baxter Healthcare Corporation
- recall number
- Z-3065-2026
- source status
- Open, Classified
- freshness minutes
- 180
Source use policy · openFDA reference data; not a real-time public alert service
Update history (1 recent revisions)
- 10/8/2026, 2:10:44 AM UTC
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