Serious health hazard — there is a reasonable probability that use of or exposure to this product will cause serious adverse health consequences or death.
BD Alaris Systems Manager Recalled by CareFusion 303, Inc. Due to Software issue that may result in outdated automated...
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
BD Alaris Systems Manager , REF 9601 Infusion Safety Management Software
Why Was This Recalled?
Software issue that may result in outdated automated programming request(APR) being sent to the progressive care unit (PCU).
Where Was This Sold?
This product was distributed to 21 states: AZ, CA, FL, GA, IL, IN, MI, MO, NJ, NY, NC, OH, OR, PA, SC, TX, UT, VA, WA, WI, DC
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