Reported Mar 19, 2025 · Ongoing
BD Alaris Systems Manager , REF 9601 Infusion Safety Management Software
CareFusion 303, Inc.
High riskUsing this product could cause serious injury, illness or death — stop using it now.What you should do
Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.
Firm contact: CareFusion 303, Inc. · 10020 Pacific Mesa Blvd · San Diego, CA · 92121-4386
Is this the product you have?
- BD Alaris Systems Manager , REF 9601 Infusion Safety Management Software
- Lot codes and dates
Software v12.5.1 or v12.5.2and prior versions (4.3312.0.112.0.212.112.1.212.3)
- UDIs10885403960123 10885403519666 (10885403960116)
This recall covers 2 products
The agency filed one notice per product. You are reading one of them; the other one is below.
Where it was sold
Why it was recalled
Stop using this product now
Software issue that may result in outdated automated programming request(APR) being sent to the progressive care unit (PCU).
Using this product could cause serious injury, illness or death — stop using it now.
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The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.
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