Class II

Medical Device Recall: BD Alaris System Manager REF: 9601, compatible with BD Alaris PC Units

CareFusion 303, Inc. · May 21, 2024

Reason for Recall

Due to a software issue the PC unit may not connect to the server which could impact wireless data transmission to and from the server.

Distribution

US Nationwide distribution including in the states of AL, AR, AZ, CA, CO, CT DC, DE, FL, GA, IA, ID, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MS, MT, NC, NE, NH, NJ, NM, NV, NY, OH, OK, OR, PA, PR, SC, SD, TN, TX, UT, VA, WA, WI.

States Affected

NATIONWIDE

Quantity Affected

168 software version

Source: FDA (openFDA Device Enforcement)

Recall number: Z-2262-2024

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.