Recall
FDAHealthJune 30, 2026

Baxter Healthcare Corporation — Baxter Duo-Vent Solution Set and Male Luer Lock Adapter, Product Code 1C8507; Solution Administration Sets

⚠️ 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.

Is this relevant to me?

Geography
Nationwide
Source agency
FDA
Category
Health
Published
June 30, 2026

US Nationwide. No OUS consignees.

What's affected?

Product
Baxter Duo-Vent Solution Set and Male Luer Lock Adapter, Product Code 1C8507; Solution Administration Sets
Lot code
DR26C27062

Additional details

UDI/DI 00085412014319, Lot Numbers: DR26C27062, exp. 30-MAR-2028; DR26D14031, exp. 15-Apr-2028; DR26E13055, exp. 14-May-2028

What should I do?

Recommended action

Class I recall. Voluntary: Firm initiated Quantity affected: 24528 units.

View original FDA notice →

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