Baxter Duo-Vent Solution Set and Male Luer Lock Adapter, Product Code 1C8507; Solution Administration Sets
Why it was recalled
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.
What to do
The recall is ongoing. Follow the firm and FDA instructions.
Affected products and identifiers
UDI/DI 00085412014319, Lot Numbers: DR26C27062, exp. 30-MAR-2028; DR26D14031, exp. 15-Apr-2028; DR26E13055, exp. 14-May-2028 — 24528 units
Record details
Baxter Healthcare Corporation — US Nationwide. No OUS consignees.