FDA Device recall Z-2766-2026
Baxter Duo-Vent Solution Set and Male Luer Lock Adapter, Product Code 1C8507
- FDA Device
- Class I
- ongoing
- Published 2026-08-19
On 2026-08-19 the FDA classified a Class I recall of Baxter Duo-Vent Solution Set and Male Luer Lock Adapter, Product Code 1C8507 by Baxter Healthcare, citing 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.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2766-2026 |
| Classification | Class I |
| Status | ongoing |
| Initiated | 2026-06-30 |
| Published | 2026-08-19 |
| Last updated | 2026-09-13 11:58 UTC |
| Company | Baxter Healthcare |
| Distribution | US |
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.
Identifiers
| code_info | UDI/DI 00085412014319, Lot Numbers: DR26C27062, exp. 30-MAR-2028; DR26D14031, exp. 15-Apr-2028; DR26E13055, exp. 14-May-2028 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:58 UTC. Current status: ongoing.
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Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2766-2026%22
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