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 Disconnections and leakages at the connection of the...
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, intravascular administration set.
Quantity: 7,700 units
Why Was This Recalled?
Disconnections and leakages at the connection of the smallbore tubing and the SmartSite Y-port.
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