FDA Recall: Software anomalies that may result in a blank Run screen

Company: Baxter Healthcare Corporation
Date of Enforcement Report: 8/29/2025
Class: I

PRODUCT

Novum IQ LVP (Large Volume Pump), Product Code 40700BAXUS, infusion pump

Recall Number:

Z-2332-2025

REASON:

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).

RECALLING FIRM/MANUFACTURER:

Baxter Healthcare Corporation

VOLUME:

43,922 units

DISTRIBUTION:

US distribution including Puerto Rico and OUS (International) Canada

About the author

Allison joined SoftwareCPR in 2022, bringing along over ten years of passion for building teamwork and growth in organizations. This is established in part by the greatest University the South has to offer- Mississippi State.

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