Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Alaris Syringe Module Model 8110 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 Syringe Module Model 8110, a modular infusion pump and monitoring system
Quantity: 20145
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