The Recall Desk

FDA (Devices) recall action 96323

CareFusion 303, Inc. recalled 2 products on 2025-03-19

The FDA (Devices) publishes a recall like this one as 2 separate product records. They share a firm, a date and a cause; this page is all of them in one place, so the scale of the action is visible rather than spread across 2 pages.

Products
2
Announced
2025-03-19
Critical
0
Units
—

Why these products were recalled

Software issue that may result in outdated automated programming request(APR) being sent to the progressive care unit (PCU).

The agency’s own wording, quoted from the enforcement report.

States named across these recalls

1–2 of 2

  • SevereFDA (Devices)··2025-03-19

    BD Care Coordination Engine Software May Send Outdated Programming Requests

    BD Care Coordination Engine infusion software may send outdated automated programming requests to care units. Healthcare facilities in affected US states should review their systems.

    Product
    BD Care Coordination Engine (CCE) Infusion Adapter, Safety Management Software
    Category
    Distribution
    21 states