Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
SmartSite Extension Set Recalled by CareFusion 303, Inc. Due to CareFusion is recalling the SmartSite Extension Set due...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact CareFusion 303, Inc. directly.
Affected Products
SmartSite Extension Set, Model No. 20029E. Used to administer fluid and medications through a needle or catheter inserted into the patient's artery or vein.
Quantity: 21,000 units
Why Was This Recalled?
CareFusion is recalling the SmartSite Extension Set due to disconnection and leakage issues.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About CareFusion 303, Inc.
CareFusion 303, Inc. has 163 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report