Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
CareFusion SmartSite Gravity Blood Set Model 42082E. Used to administer Recalled by Carefusion 303 Inc Due to CareFusion is recalling the SmartSite¿ Gravity Blood Set...
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
CareFusion SmartSite Gravity Blood Set Model 42082E. Used to administer blood and blood products through a needle or catheter inserted into the patient's artery or vein.
Quantity: 5,050 units
Why Was This Recalled?
CareFusion is recalling the SmartSite¿ Gravity Blood Set as a result of a potential for separation at the connection of the drip chamber and tubing . The separation may be observed at priming or observed during use. If a separation between the drip chamber and tubing occurs, this could cause a delay in treatment.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Carefusion 303 Inc
Carefusion 303 Inc has 1 total recall tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report