CareFusion 303, Inc. recalls BD Alaris Systems Manager , REF 9601 Infusion Safety Managem
Recalled Product
BD Alaris Systems Manager , REF 9601 Infusion Safety Management Software
Hazard / Issue
Software issue that may result in outdated automated programming request(APR) being sent to the progressive care unit (PCU).
Issued by
FDA
Affected States: AZ, CA, DC, FL, GA, IL, IN, MI, MO, NC, NJ, NY, OH, OR, PA, SC, TX, UT, VA, WA, WI
Lot/Code Info: Software v12.5.1 or v12.5.2, and prior versions (4.33, 12.0.1, 12.0.2, 12.1, 12.1.2, 12.3) UDIs: 10885403960123 10885403519666 (10885403960116)
View official government recall
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