Device recall

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

FDA recall source

Recall number

Z-2766-2026

Event id

99343

Status

Ongoing

FDA classification

Class I

Recalling firm

Baxter Healthcare Corporation

Report date

Aug 19, 2026

Initiated

Jun 30, 2026

Center classification date

Aug 11, 2026

Reason

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.

Quantity

24528 units

Code info

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

Distribution

US Nationwide. No OUS consignees.

Voluntary or mandated

Voluntary: Firm initiated

Location

Deerfield, IL, United States