Class I
Medical Device Recall: Baxter Duo-Vent Solution Set and Male Luer Lock Adapter, Product Code 1C8507; Solution Administration Sets
Baxter Healthcare Corporation · June 30, 2026
Reason for Recall
Baxter received customer reports of air bubbles in the drip chamber and tubing when a pressure cuff is in use or when the tubing is flushed at the fully open position.
Distribution
US Nationwide. No OUS consignees.
States Affected
NATIONWIDE
Quantity Affected
24528 units
Source: FDA (openFDA Device Enforcement)
Recall number: Z-2766-2026
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.