Class II

Medical Device Recall: Baxter Continu-Flo Solution Set with Duo-Vent Spike, REF UC8519

Baxter Healthcare Corporation · December 20, 2024

Reason for Recall

Specific lots of Solution Sets with Duo-Vent Spike have the potential for inverted side clamps causing the tubing to be unusable.

Distribution

US Nationwide distribution in the states of MN, MO, VA, TX, CA, MA, FL, SC.

States Affected

NATIONWIDE

Source: FDA (openFDA Device Enforcement)

Recall number: Z-1011-2025

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.