Class II

Medical Device Recall: Baxter Spectrum IQ Infusion System with Dose IQ Safety Software, Product Code 3570009

Baxter Healthcare Corporation · October 2, 2024

Reason for Recall

The door on the Spectrum IQ Infusion pump may not be able to fully close.

Distribution

GA, ID

States Affected

GA, ID

Quantity Affected

8 units

Source: FDA (openFDA Device Enforcement)

Recall number: Z-0348-2025

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 Spectrum IQ Infusion System with Dose IQ Safety Software, Product Code 3570009 | SafeCheck