Class I

Medical Device Recall: BD Alaris Systems Manager , REF 9601 Infusion Safety Management Software

CareFusion 303, Inc. · February 18, 2025

Reason for Recall

Software issue that may result in outdated automated programming request(APR) being sent to the progressive care unit (PCU).

Distribution

US: AZ, CA, DC, FL, GA, IL, IN, MI, MO, NC, NJ, NY, OH, OR, PA, SC, TX, UT, VA, WA, WI OUS: None

States Affected

AZ, CA, DC, FL, GA, IL, IN, MI, MO, NC, NJ, NY, OH, OR, PA, SC, TX, UT, VA, WA, WI

Source: FDA (openFDA Device Enforcement)

Recall number: Z-1304-2025

Status: ongoing

SafeCheck provides drug interaction information from FDA-approved product labeling (openFDA). This is for informational purposes only and is not medical advice. Always consult your healthcare provider before making medication decisions.