Baxter Healthcare Corporation: Set, Administration, Intravascular
Baxter Healthcare Recall Summary Baxter Healthcare is recalling Duo-Vent Solution Sets and Male Luer Lock Adapters (Product Code 1C8507) distributed nationwide in the US because air bubbles can form in the drip chamber and tubing when a pressure cuff is used or tubing is flushed at full opening. This is a Class II recall, meaning there is potential for serious adverse health effects. The recall affects intravenous administration products that were distributed across all US states.
- Recalling firm
- Baxter Healthcare Corporation
- 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.
- Classification
- Class II
- Category
- medical device recall
- Country
- United States
- Agency
- FDA-DEVICES
- Recall date
- 2026-06-30
- Status
- Open, Classified
- Areas affected
- AL, AK, AZ, AR, CA, CO, CT, DE, FL, GA, HI, ID, ...
- Distribution
- US Nationwide. No OUS consignees.
Official recall notice from FDA-DEVICES
Recall details on Nibble Recalls: https://trynibble.app/recalls/e5e9f3fa-4229-4b48-af8a-e9766fbd6b82