Baxter Healthcare Corporation: Medical Device Recall in 2025 - (Recall #: Z-1964-2025)

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:

Baxter Novum IQ Syringe Pump, product code 40800BAXUS,

Product Classification:

Class II

Date Initiated: May 12, 2025

Date Posted: June 18, 2025

Recall Number: Z-1964-2025

Event ID: 96822

Reason for Recall:

Baxter has identified a design issue which may cause the pump to detect the presence of a syringe flange when no syringe is loaded. When this issue occurs, the pumps 'user interface becomes stuck on the "Remove Syringe" screen when an infusion is complete, and the syringe is unloaded. A System Error 21502 (Flange Sensor Failure) may occur. Please note this issue only affects a subset of Novum IQ syringe pumps manufactured or repaired after July 4, 2023.

Status: Ongoing

Product Quantity: 8027 units

Code Information:

UDI/DI 05413765852428, All Serial Numbers

Distribution Pattern:

US Nationwide distribution.

Voluntary or Mandated:

Voluntary: Firm initiated