Baxter Healthcare Corporation: Medical Device Recall in 2025 - (Recall #: Z-2333-2025)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2025.

Data Source: FDA.

Product Description:

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

Product Classification:

Class I

Date Initiated: August 4, 2025

Date Posted: September 10, 2025

Recall Number: Z-2333-2025

Event ID: 97296

Reason for Recall:

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).

Status: Ongoing

Product Quantity: 10,101 units

Code Information:

UDI/DI 05413765852428, All Serial Numbers

Distribution Pattern:

US distribution including Puerto Rico and OUS (International) Canada

Voluntary or Mandated:

Voluntary: Firm initiated