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.
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.
Air bubbles can form in the drip chamber when the pressure cuff is in use or when the tubing is flushed at the fully open position. This may lead to incorrect medication delivery if the air bubbles are not properly managed during medical procedures.
Healthcare professionals using these medical devices for patient care are most likely affected. Patients receiving treatment with these devices may also be impacted if air bubbles cause medication errors.
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).
Look for product code 1C8507 on the Duo-Vent Solution Set and Male Luer Lock Adapter.
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.
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).
The recall record does not specify a remedy.
We’ve drafted a message you can send Baxter to request your refund or repair — edit it as you like.
Subject: Recall Z-2766-2026 — Baxter Baxter Hello, I own a Baxter that is covered by recall Z-2766-2026 from Baxter. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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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.
