Product Wiki · Recalls · U.S. FDA — Device Enforcement

BD Alaris Systems Manager , REF 9601 Infusion Safety Management Software — recall Z-1304-2025

U.S. FDA — Device Enforcement · United States · 2025-02-18 · Class I

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-1304-2025
Date of alert
2025-02-18
Country / jurisdiction
United States
Risk level
Class I
Risk type
recall
Brand
CareFusion 303, Inc.
Product category
device
Product type
Devices
Barcode (EAN/GTIN)
10885403960123
Reported risk: Software issue that may result in outdated automated programming request(APR) being sent to the progressive care unit (PCU).
Primary source: https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?start_search=1&

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