Baxter Duo-Vent Solution Set and Male Luer Lock Adapter recall
Baxter Healthcare Corporation recalled Baxter Duo-Vent Solution Set and Male Luer Lock Adapter on August 19, 2026 because of 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. It was sold nationwide.
Why it was recalled
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.
What's recalled
Baxter Duo-Vent Solution Set and Male Luer Lock Adapter, Product Code 1C8507; Solution Administration Sets
Quantity: 24528 units
What to do
Check whether you have the product (match the lot numbers, dates or codes in the official notice). Stop using it, and return it or throw it away as the notice says.
Read the official FDA noticeDetails
- Company
- Baxter Healthcare Corporation, Deerfield, IL
- Date
- Severity
- Class I · most serious
the most serious: the product could cause serious health problems or death. - Where sold
- Nationwide
US Nationwide. No OUS consignees. - Status
- Ongoing
- Recall number
- Z-2766-2026
- Source
- U.S. Food and Drug Administration
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