Class I

Medical Device Recall: Novum IQ Syringe Pump, Product Code 40800BAXUS, infusion pump

Baxter Healthcare Corporation · August 4, 2025

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).

Distribution

US distribution including Puerto Rico and OUS (International) Canada

Quantity Affected

10,101 units

Source: FDA (openFDA Device Enforcement)

Recall number: Z-2333-2025

Status: ongoing

SafeCheck provides drug interaction information from FDA-approved product labeling (openFDA). This is for informational purposes only and is not medical advice. Always consult your healthcare provider before making medication decisions.

Baxter Healthcare Corporation Medical Device Recall: Novum IQ Syringe Pump, Product Code 40800BAXUS, infusion pump | SafeCheck