Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
MaxPlusTM bi fuse extension set with 2 clear needleless connectors Recalled by CAREFUSION Due to A portion of a validation lot was inadvertently...
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 directly.
Affected Products
MaxPlusTM bi fuse extension set with 2 clear needleless connectors - Product Usage: The needleless connector can be used for direct injection, intermittent infusion, continuous infusion, or aspiration.
Quantity: 100 units
Why Was This Recalled?
A portion of a validation lot was inadvertently released to the US Market. The product did not meet the validation testing criteria regarding leakage.
Where Was This Sold?
This product was distributed to 1 state: TN
About CAREFUSION
CAREFUSION has 25 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report