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FDA · Medical devices ·

Baxter Novum IQ Syringe Pump recall

Baxter Healthcare Corporation recalled Baxter Novum IQ Syringe Pump on September 9, 2026 because of 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. It was sold nationwide.

Why it was recalled

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's recalled

Baxter Novum IQ Syringe Pump, Model Number 40800BAXUS

Quantity: 14601 units

What to do

Check whether you have the product (match the lot numbers, dates or codes in the official notice). Stop using it, and return it or throw it away as the notice says.

Read the official FDA notice

Details

Company
Baxter Healthcare Corporation, Deerfield, IL
Date
Severity
Class II
the product could cause temporary or reversible health problems.
Where sold
Nationwide
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
Recall number
Z-3065-2026
Source
U.S. Food and Drug Administration

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