Baxter Healthcare Corporation Duo-Vent Solution Set Recall (March 2028)
Announced 2026-08-19 · FDA
FDA recall of Baxter Duo-Vent Solution Set and Male Luer Lock Adapter (Product Code 1C8507; Solution Administration Sets) due to 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. About 24,528 units distributed nationwide in the United States are affected; the affected lots are DR26C27062 (exp 30-MAR-2028), DR26D14031 (exp 15-APR-2028), and DR26E13055 (exp 14-MAY-2028).
| Brand | Baxter Healthcare Corporation |
|---|---|
| Product | Baxter Duo-Vent Solution Set and Male Luer Lock Adapter, Product Code 1C8507; Solution Administration Sets |
| Reason | 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. |
| Severity | critical |
| Units affected | 24528 units |
| Distribution | US Nationwide. No OUS consignees. |
| Agency | FDA |
| Recall / campaign no. | UDI/DI 00085412014319, Lot Numbers: DR26C27062, exp. 30-MAR-2028; DR26D14031, exp. 15-Apr-2028; DR26E13055, exp. 14-May-2028 |
WHAT YOU SHOULD DO
- Do not use affected Baxter Duo-Vent solution sets or adapters.
- Check if your device lot number matches DR26C27062, DR26D14031, or DR26E13055.
- Contact your healthcare provider or Baxter for replacement/return instructions.
- Follow any recall-specific instructions provided by the FDA.
This is an automatically maintained record of an official recall notice. Details can change; always follow the official notice linked above. See all records in the Recall Database.