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Baxter Healthcare Corporation Recall

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

Updated June 30, 2026

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

Is the Baxter Healthcare Corporation recalled? Yes. This product was recalled by FDA on June 30, 2026. Details below.

What is recalled

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

Am I affected

You may be affected if you own this product. Check the brand, model, and lot/date codes listed in the recall against your item.

What to do right now

Voluntary: Firm initiated

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.

Brands affected

Baxter Healthcare Corporation
Source
FDA
Category
Drugs & Medications
Recall ID
fda-Z-2766-2026
Classification
Class I
Recalled
June 30, 2026
Read the official notice

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