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CareFusion 303, Inc. recalls BD Alaris Systems Manager , REF 9601 Infusion Safety Management Software
Recalled March 19, 2025 · FDA recall Z-1304-2025 · CareFusion 303
Hazard
Software issue that may result in outdated automated programming request(APR) being sent to the progressive care unit (PCU). · FDA Class I
Sold at
US: AZ, CA, DC, FL, GA, IL, IN, MI, MO, NC, NJ, NY, OH, OR, PA, SC, TX, UT, VA, WA, WI OUS: None
Description
Software issue that may result in outdated automated programming request(APR) being sent to the progressive care unit (PCU).
Product
BD Alaris Systems Manager , REF 9601 Infusion Safety Management Software
Manufacturer(s)
CareFusion 303, Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →