Baxter Duo-Vent Solution Set and Male Luer Lock Adapter — Class I medical device recall Z-2766-2026
Ongoing recall by Baxter Healthcare Corporation, reported 2026-08-19, distributed nationwide. Baxter received customer reports of air bubbles in the drip chamber and tubing when a pressure cuff is in use
| Recall number | Z-2766-2026 |
|---|---|
| Product type | Medical device |
| Classification | Class I |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | Baxter Healthcare Corporation, Deerfield, IL, United States |
| Recall initiated | 2026-06-30 |
| Classified | 2026-08-11 |
| Reported by FDA | 2026-08-19 |
| Distributed | Nationwide (US) |
| Quantity | 24,528 units |
| UPC / GTIN / UDI-DI | 00085412014319 |
| Lot numbers | DR26C27062, DR26D14031, DR26E13055 |
| Expiration dates | 2028-03-30, 2028-04-15, 2028-05-14 |
Product
Baxter Duo-Vent Solution Set and Male Luer Lock Adapter, Product Code 1C8507; Solution Administration Sets
Reason for recall
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.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-2766-2026. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.