Baxter Healthcare Corporation: Medical Device Recall in 2023 - (Recall #: Z-0151-2024)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2023.

Data Source: FDA.

Product Description:

Novum IQ Syringe infusion system, Product Code 40800BAXUS

Product Classification:

Class I

Date Initiated: October 13, 2023

Date Posted: November 15, 2023

Recall Number: Z-0151-2024

Event ID: 93191

Reason for Recall:

Baxter is issuing an Urgent Medical Device Correction for the Novum IQ Syringe Pump. Baxter identified that after multiple downstream occlusion alarms, the pump may display an Infusion Complete alarm even though uninfused fluid remains in the syringe.

Status: Ongoing

Product Quantity: 2023 units

Code Information:

All Serial Numbers

Distribution Pattern:

US Nationwide Distribution to states of: AR, AZ, CA, FL, GA, HI, IA, IN, KS, LA, MD, MI, MN, MO, NC, NE, NH, NJ, NY, PA, TX, UT, VA, VT, WA, WI AND WV.

Voluntary or Mandated:

Voluntary: Firm initiated