Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Alaris PC units Recalled by CareFusion 303, Inc. Due to CareFusion is recalling the Alaris PC unit because...
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
Alaris PC units, Model No. 8015. Infusion pump.
Quantity: 56,015 units
Why Was This Recalled?
CareFusion is recalling the Alaris PC unit because of an error code. The error code may occur upon power on during the "Power-On Self Test" due to a keypad issue.
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