United StatesBaxter Novum IQ Syringe Pump (Model 40800BAXUS) and Baxter Novum IQ Syringe Pump, Loaner (Model 40800BAXUSL) with UDI‑DI 05413765852428 (all serial numbers) and UDI‑DI 00197886002300 (all serial numbers) are affected. They were recalled because a software issue may occur during a Volume/Time multi‑syringe infusion when a syringe reaches empty and is replaced while a Volume To Be Infused (VTBI) remains.
What's being recalled
Baxter Novum IQ Syringe Pump, Model Number 40800BAXUS
Baxter Novum IQ Syringe Pump, Loaner, Model Number 40800BAXUSL
Recalling firm: Baxter Healthcare Corporation, Deerfield, IL, United States.
How to identify it
UDI-DI 05413765852428, all serial numbers UDI-DI 00197886002300, all serial numbers
The 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.
What to do
Don't stop taking a prescribed medicine without talking to your doctor or pharmacist first. For other products, stop using them and ask the pharmacist, seller or maker what to do.
The notice doesn't give instructions for consumers, so this is general advice for health & beauty recalls. Check the official notice for the details.
Where it was sold
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.
The official notice
This page is a summary of the notice published by U.S. Food and Drug Administration (enforcement reports), collected from U.S. Food and Drug Administration (enforcement reports). Check the original before you act on it.
Read the official notice (opens in a new tab)