Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
SmartSite Low Sorbing Infusion Set Recalled by CareFusion 303, Inc. Due to CareFusion is recalling the SmartSite Low Sorbing Infusion...
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 Low Sorbing Infusion Set, Model Codes: 10014855A, 10015861A, 10061661A 14035457 14035485 14046894 14035458
Quantity: 5,600 units
Why Was This Recalled?
CareFusion is recalling the SmartSite Low Sorbing Infusion Set because they were assembled with a drip chamber that consist of a 15 micron filter. The Directions For Use did not indicate that the drip chamber has a 15 micron filter and it does not provide the instruction that the set should not be used with blood administration due to the potential for occluding the 15 micron filter in the drip c
Where Was This Sold?
This product was distributed to 5 states: FL, NM, TX, WA, WI
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