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# CareFusion Recalls BD Alaris Systems Manager
- URL: https://www.fdaweb.com/carefusion-recalls-bd-alaris-systems-manager/
- Published: 2025-03-14T12:00:00.000Z
- Updated: 2026-09-14T14:55:23.000Z
- Author: David McFarland
- Tags: Devices, #legacy-id-D5158827

Becton Dickinson’s CareFusion unit has recalled (Class 1) its BD Alaris Systems Manager, including the device’s infusion safety management software, due to software issues that could provide incorrect therapy. The software issue may result in an outdated automated programming request being sent to the device’s progressive care unit, a [recall notice](https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfres/res.cfm?id=212551&ref=fdaweb.com) says. Last month, the company sent an “Urgent Medical Device Product Correction” letter to users that advised them to review all infusion parameters pre-populated and confirm they are correct before pressing “Start” to commence therapy.