United StatesBaxter Duo-Vent Solution Set and Male Luer Lock Adapter (Solution Administration Sets), Product Code 1C8507, UDI/DI 00085412014319, Lot DR26C27062 (exp. 30-MAR-2028), DR26D14031 (exp. 15-APR-2028), and DR26E13055 (exp. 14-MAY-2028), sold nationwide in the United States, are affected. Baxter is recalling these units after 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's being recalled
Baxter Duo-Vent Solution Set and Male Luer Lock Adapter, Product Code 1C8507; Solution Administration Sets
Recalling firm: Baxter Healthcare Corporation, Deerfield, IL, United States.
How to identify it
UDI/DI 00085412014319, Lot Numbers: DR26C27062, exp. 30-MAR-2028; DR26D14031, exp. 15-Apr-2028; DR26E13055, exp. 14-May-2028
The hazard
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
Don't stop taking a prescribed medicine without talking to your doctor or pharmacist first. For other products, stop using them and ask the pharmacist, seller or maker what to do.
The notice doesn't give instructions for consumers, so this is general advice for health & beauty recalls. Check the official notice for the details.
Where it was sold
US Nationwide. No OUS consignees.
The official notice
This page is a summary of the notice published by U.S. Food and Drug Administration (enforcement reports), collected from U.S. Food and Drug Administration (enforcement reports). Check the original before you act on it.
Read the official notice (opens in a new tab)