Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Alaris System PC unit Recalled by CareFusion 303, Inc. Due to Reports where the Low Battery alarm and/or the...
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 no. 8000 and 8015. The central programming, monitoring and power supply component for the Alaris infusion pump System.
Quantity: 613,800 total units (575,221 units in US)
Why Was This Recalled?
Reports where the Low Battery alarm and/or the Very Low Battery alarm are not being triggered before the battery is discharged and all infusion channels are stopped.
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