Baxter Duo-Vent Solution Set and Male Luer Lock Adapter, Product Code 1C8507; 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.
| Recalling firm | Baxter Healthcare Corporation |
|---|---|
| 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. |
| Risk class | Class I (Class I · high risk) |
| Status | Ongoing |
| Report date | Aug 19, 2026 |
| Initiated | Jun 30, 2026 |
| Region | IL, United States |
| Distribution | US Nationwide. No OUS consignees. |
| Quantity | 24528 units |
| Code/Lot | UDI/DI 00085412014319, Lot Numbers: DR26C27062, exp. 30-MAR-2028; DR26D14031, exp. 15-Apr-2028; DR26E13055, exp. 14-May-2028 |
| Type | Voluntary: Firm initiated |
| Recall number | Z-2766-2026 |
Official source
U.S. FDA — Recalls, Market Withdrawals & Safety Alerts fda.gov ↗You can re-verify each item on the official FDA site using its recall number. (Recall number: Z-2766-2026)
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