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 - a modular infusion pump and monitoring system Recalled by CareFusion 303, Inc. Due to Due to affected devices that may have bent...
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 - a modular infusion pump and monitoring system
Quantity: 125017 device (finished devices and kits)
Why Was This Recalled?
Due to affected devices that may have bent female IUI connector and may not be operable and potentially cause delays in the start of the infusion or monitoring.
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