Lower riskMedical device recall · FDA · Published June 30, 2026
Baxter Duo-Vent Solution Set Recall: Air Bubbles When Pressure Cuff Used
Baxter recalls Duo-Vent Solution Sets with air bubbles in drip chamber when pressure cuff is used or tubing flushed fully open. Affected units have specific product codes and expiration dates.
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.
✎ GovInfoNow plain-language explainer
Baxter is recalling certain Duo-Vent Solution Sets and Male Luer Lock Adapters due to air bubbles forming in the drip chamber when a pressure cuff is used or when the tubing is flushed at the fully open position. This could lead to incorrect medication delivery if the air bubbles are not properly managed during medical procedures. Read more at govinfonow.com/recall/459439-baxter-duo-vent-solution-set-recall-air-bubbles-when-pressure.
“Baxter Duo-Vent Solution Set Recall: Air Bubbles When Pressure Cuff Used.” GovInfoNow, updated August 27, 2026. https://govinfonow.com/recall/459439-baxter-duo-vent-solution-set-recall-air-bubbles-when-pressure. Based on FDA recall #Z-2766-2026 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2766-2026%22&limit=1).
The FDA announced on June 30, 2026, that Baxter Healthcare Corporation is voluntarily recalling its Duo-Vent Solution Set and Male Luer Lock Adapter due to air bubble hazards. The recall affects approximately 24,528 units distributed nationwide.
How to tell if you have it
Brand: Baxter
Product: Duo-Vent Solution Set and Male Luer Lock Adapter; Solution Administration Sets
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. The recall is classified as Class I.
Context
GovInfoNow's records show Baxter Healthcare Corporation has 187 other recalls on record since September 2, 2015. Other recent recalls of similar products include PRO+ 36" MRS SURFACE (August 18, 2026), 0.9% Sodium Chloride Injection (August 17, 2026), and Dextrose 2000mL Bags (August 17, 2026). Other recent recalls of similar products include ICU Medical CADD Yellow Medication Cassette Reservoir (August 20, 2026) and B Braun Hemodialysis Bloodlines (March 19, 2026).
How to tell if you have this one
Check for product code 1C8507 on the Duo-Vent Solution Set and Male Luer Lock Adapter. Affected units have specific lot numbers: DR26C27062 (expires 30-MAR-2028), DR26D14031 (expires 15-Apr-2028), or DR26E13055 (expires 14-May-2028).
Brand
Baxter
Category
Medical device
Based on the official FDA remedy
What to do — step by step
Check Product Code
Look for product code 1C8507 on the Duo-Vent Solution Set and Male Luer Lock Adapter.
Where it went and when
Where it was distributed
Distributed nationwide.
Nationwide
Not listed
FDA distribution: “US Nationwide. No OUS consignees.” States read from FDA’s own wording; “not listed” means the notice does not name it.
Distributed nationwide.
Recall timeline
FDA published this recall 50 days after the firm started it.
1Firm started the recall
2FDA classified it Class I
3Published in FDA’s Enforcement Report
4Added to GovInfoNow
Dates from the agency record only; steps without a date are left out.
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
Official source: FDA Recall #Z-2766-2026 (June 30, 2026) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-2766-2026 to see it in context.
Plain-language summary written by qwen3:4b on August 27, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.