FDA recall record

Baxter Duo-Vent Solution Set and Male Luer Lock Adapter, Product Code 1C8507 recall — FDA Z-2766-2026

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…

Class Iclassification
Z-2766-2026official record ID
Aug 19, 2026report date

Recall record at a glance

Official recordZ-2766-2026
CategoryMedical Device Recalls
ClassificationClass I
FDA record statusOngoing
Recalling firmBaxter Healthcare Corporation
Report dateAug 19, 2026
Recall initiation dateJun 30, 2026
Quantity24528 units
LocationDeerfield, IL, United States

Official product description

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

Why the product was recalled

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.

Distribution information

US Nationwide. No OUS consignees.

How to read the classification

FDA Class I indicates a situation in which there is a reasonable probability that use of or exposure to the product will cause serious adverse health consequences or death. The classification shown here comes directly from the FDA enforcement record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Letter.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

Recall Lookup USA preserves the most complete source information successfully retrieved. We do not create missing facts or infer affected lots or VINs. The official record may still change, so use the identifier above when verifying current instructions.

FDA source limitation: openFDA enforcement reports are a reference dataset, not a live public-alert or recall-lifecycle service. FDA notes that enforcement-report status may not be updated after classification. Confirm current actions with the FDA, recalling firm or appropriate healthcare professional when relevant.

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Class IIFDA: OngoingBaxter Healthcare Corporation