Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Alaris Pump Module model 8100 Recalled by CareFusion 303, Inc. Due to There is a potential risk that could cause...
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 Pump Module model 8100
Quantity: 35,940 units
Why Was This Recalled?
There is a potential risk that could cause unintended flow in the older, centered sear door latch design in the Alaris Pump module model 8100.
Where Was This Sold?
US and Canada
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