Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Alaris PCA Module Model 8120 - Product Usage: is intended Recalled by CareFusion 303, Inc. Due to LED display, which provides infusion or patient monitoring...
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 PCA Module Model 8120 - Product Usage: is intended to provide trained healthcare caregivers a way to automate the programming of infusion parameters, thereby decreasing the amount of manual steps necessary to enter infusion data.
Quantity: 89497
Why Was This Recalled?
LED display, which provides infusion or patient monitoring values, on the module may have segments that appear dim.
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