- Recalling firm
- Baxter Healthcare Corporation
- 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.
- Affected products (lot / model / serial)
- UDI/DI 00085412014319, Lot Numbers: DR26C27062, exp. 30-MAR-2028; DR26D14031, exp. 15-Apr-2028; DR26E13055, exp. 14-May-2028
- Units affected
- 24528 units
- Distribution pattern
- US Nationwide. No OUS consignees.
- Firm location
- Deerfield, IL, United States
- Recall type
- Voluntary: Firm initiated
- How the firm notified customers
- Letter
- Product type
- Devices
- Status
- Ongoing
- Recall number
- Z-2766-2026
- Recall initiated
- June 30, 2026
- FDA classification date
- August 11, 2026
- FDA report date
- August 19, 2026
- FDA event ID
- 99343
- Last updated on HTM Vibe
- August 26, 2026