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Food and Drug Administration · Recall Z-2766-2026 · Jun 30, 2026

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

Baxter Healthcare Corporation

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. FDA Class I recall.

The remedy

Follow FDA guidance

About this recall

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

Affected identifiers

Check these against the label on your unit. An identifier match is how a recall is confirmed, not just suspected.

Model UDI/DI 00085412014319Model Lot Numbers: DR26C27062Model exp. 30-MAR-2028Model DR26D14031Model exp. 15-Apr-2028Model DR26E13055Model exp. 14-May-2028UPC 00085412014319

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Sourced from the Food and Drug Administration’s public recall data. Always verify serial and date ranges against the official notice before acting.