Z-2766-2026 Class I Ongoing
FDA device recall Z-2766-2026 was initiated by Baxter Healthcare Corporation on Jun 30, 2026 and is designated Class I. 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. The recall status is ongoing. Affected quantity: 24528 units.
Recall details
- Product Type
- Devices
- Report Date
- Aug 19, 2026
- Initiation Date
- Jun 30, 2026
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 24528 units
Product description
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.
Distribution pattern
US Nationwide. No OUS consignees.
Code information
UDI/DI 00085412014319, Lot Numbers: DR26C27062, exp. 30-MAR-2028; DR26D14031, exp. 15-Apr-2028; DR26E13055, exp. 14-May-2028
Source
- Dataset
- openFDA device recall enforcement reports
- FDA record
- This recall in openFDA (JSON)
- Enforcement Report
- Search FDA's Enforcement Report for Z-2766-2026
- openFDA file date
- Nov 10, 2026
- Loaded by RegDataLab
- Nov 11, 2026