Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Alaris System PC Unit Model 8015 with software versions 9.17 and 9.19 Recalled by CareFusion 303, Inc. Due to A patient weight can be populated incorrectly under...
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 System PC Unit Model 8015 with software versions 9.17 and 9.19; Central programming, monitoring and power supply component for the Alaris System.
Quantity: 69,693 units
Why Was This Recalled?
A patient weight can be populated incorrectly under certain conditions when using the RESTORE feature to restore infusions running on the Alaris LVP module model 8100 and the Alaris Syringe module model 8110.
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