Critical Alert
Baxter Healthcare Corporation Recalls Baxter Duo-Vent Solution Set and Male Luer Lock Adapter
This is a Class I recall — the most serious type. There is a reasonable probability of serious health consequences or death.
Source: FDA
CriticalRecall #Z-2766-2026Medical Device
Baxter Healthcare Corporation Recalls Baxter Duo-Vent Solution Set and Male Luer Lock Adapter
Baxter Healthcare Corporation · Class I — Most Serious
Product Description
Baxter Duo-Vent Solution Set and Male Luer Lock Adapter, Product Code 1C8507; Solution Administration Sets
Reason for Recall
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 Classification
Class I — Most Serious
A situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Distribution
US Nationwide. No OUS consignees.
Remedy
Consumers should stop using this product. Contact the recalling firm for further instructions regarding this product.
411 Press Analysis
Baxter Healthcare Corporation is recalling a medical device classified as Class I by the FDA — the highest risk level. The recall was initiated on June 30, 2026 affecting 24528 units. 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. It was distributed in US Nationwide. No OUS consignees. Consumers and healthcare professionals should exercise caution and discontinue use of the recalled product. Contact the recalling firm directly for return or disposal instructions.
Sources: FDA openFDA Enforcement Database
This recall appears in: Medical Device Defects.