Class I

Medical Device Recall: Baxter SIGMA Spectrum Infusion Pump V8, Model Number 35700BAX2

Baxter Healthcare Corporation · June 20, 2025

Reason for Recall

Certain Spectrum infusion pumps may have an incorrect version of software.

Distribution

US States: CA, FL, IL, KS, MI, MS, NY, OH, OK, and VA.

States Affected

CA, FL, IL, KS, MI, MS, NY, OH, OK, VA

Quantity Affected

28 units

Source: FDA (openFDA Device Enforcement)

Recall number: Z-2096-2025

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 SIGMA Spectrum Infusion Pump V8, Model Number 35700BAX2 | SafeCheck