Class I

Medical Device Recall: Baxter Novum IQ LVP INFUSION SYSTEM, REF 40700BAXUS

Baxter Healthcare Corporation · April 24, 2025

Reason for Recall

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.

Distribution

US and Canada

Quantity Affected

34,524 units

Source: FDA (openFDA Device Enforcement)

Recall number: Z-1767-2025

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: Baxter Novum IQ LVP INFUSION SYSTEM, REF 40700BAXUS | SafeCheck