Class I

Medical Device Recall: Baxter Sigma Spectrum Infusion System (V6 Platform), Product Code 35700BAX

Baxter Healthcare Corporation · February 5, 2025

Reason for Recall

There is the potential for missing motor mounting screws, which may have occurred during the servicing process.

Distribution

US: Nationwide

States Affected

NATIONWIDE

Quantity Affected

66 units

Source: FDA (openFDA Device Enforcement)

Recall number: Z-1253-2025

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.