Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Alaris PC unit model 8015 with software version 9.12 Product Recalled by Carefusion Corporation Due to The recall was initiated because Carefusion has identified...
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 Corporation directly.
Affected Products
Alaris PC unit model 8015 with software version 9.12 Product Usage: The Alaris PC unit is the central programming, monitoring and power supply component for the Alaris System
Quantity: 4,090 total units
Why Was This Recalled?
The recall was initiated because Carefusion has identified potential risk associated with bolus programming with the Alaris PC unit (model 8015) software version 9.12. Automating infusion pump parameter input from either the electronic medical record (EMR) or the Alaris Auto-ID module for a continuous infusion with a bolus dose option may result in a loss of information from the Guardrails Data s
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Carefusion Corporation
Carefusion Corporation has 2 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report