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Baxter Duo-Vent Solution Set
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MEDICAL DEVICE RECALLCRITICAL

Baxter Duo-Vent Solution Set

Baxter recalls Duo-Vent Solution Set (1C8507) over air bubble risk in drip chamber and tubing.

What to do

Stop using the affected Duo-Vent Solution Set and Male Luer Lock Adapter immediately. Contact Baxter Healthcare Corporation for instructions on returning the product and obtaining a replacement.

Recalled
Listed
Updated
Recall No.
Z-2766-2026
Agency
FDA
Firm
Baxter Healthcare Corporation
Recall ID
99343
Status
ONGOING

Recall at a glance

Quantity recalled
24528 units

Why it was recalled

Baxter Healthcare Corporation is recalling the Duo-Vent Solution Set and Male Luer Lock Adapter (Product Code 1C8507) because air bubbles may form in the drip chamber and tubing when a pressure cuff is in use or when the tubing is flushed at the fully open position. This can affect the accuracy of fluid delivery.

Is mine affected?

Check the model, lot, or serial number on the device or its packaging. Yours is affected if it matches one below.

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

Lot code
DR26C27062, 30-MAR-2028
UDI-DI
00085412014319

Where it was sold

Distributed nationwide.

Timeline

  1. Firm initiated recall
  2. Publicly announced
  3. Listed on Recall Canary
  4. Summary updated

Other Device Defect recalls

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Editorial summary by Recall Canary · summary updated 2026-08-12 · primary source: U.S. Food and Drug Administration · severity reflects the agency's published classification