Baxter Healthcare Corporation: Baxter Novum Iq Syringe Pump, Model Number 40800baxus
Recall Summary Baxter Healthcare is recalling the Novum IQ Syringe Pump (Model 40800BAXUS) due to a software problem that can occur when using multiple syringes in one infusion session. If a syringe empties and is replaced while medication remains to be delivered, the pump may not function correctly. The pump has been distributed nationwide across all U.S. states and territories.
- Recalling firm
- 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
- Category
- medical device recall
- Country
- United States
- Agency
- U.S. Food and Drug Administration
- Recall date
- 2026-08-11
- Status
- Ongoing
- Areas affected
- AL, AK, AZ, AR, CA, CO, CT, DE, FL, GA, HI, ID, ...
- 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.
Official recall notice from U.S. Food and Drug Administration
Recall details on Nibble Recalls: https://trynibble.app/recalls/001503ca-42d3-44ed-aa39-157c7f930e8b