Baxter Healthcare Corporation recalls Novum IQ Syringe Pump, Product Code 40800BAXUS, infusion pump

Recall date

August 4, 2025

Source

U.S. Food & Drug Administration (FDA) — enforcement report

Recall number

Z-2333-2025

FDA classification

Class I

Brand / firm

Baxter Healthcare Corporation

Sold / distributed

US distribution including Puerto Rico and OUS (International) Canada

Why it was recalled

Baxter Healthcare Corporation is issuing an Urgent Medical Device Correction for the Novum IQ Large Volume Pump (LVP) and Novum IQ Syringe Pump (SP) due to software anomalies that may result in a blank Run screen (LVP and SP) and/or false motor movement system error (SP only).

Class I is the FDA’s most serious recall level: there is a reasonable probability that using this product will cause serious harm or death.

What was recalled

Novum IQ Syringe Pump, Product Code 40800BAXUS, infusion pump