Baxter Healthcare Corporation recalls Baxter Novum IQ LVP INFUSION SYSTEM, REF 40700BAXUS

Recall date

April 24, 2025

Source

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

Recall number

Z-1767-2025

FDA classification

Class I

Brand / firm

Baxter Healthcare Corporation

Sold / distributed

US and Canada

Why it was recalled

There is a potential for the Novum IQ LVP due to the potential for underinfusion following use of the "standby mode" feature or if the device is powered off with the set loaded.

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

Baxter Novum IQ LVP INFUSION SYSTEM, REF 40700BAXUS