Reported Jan 22, 2025 · Ongoing
BD Pyxis MedStation ES (Med ES Main), REF: 323; and BD Pyxis MedStation ES (Med ES Main Tower), REF: 352
CareFusion 303, Inc.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.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 Pyxis MedStation ES (Med ES Main)
- REF323; and BD Pyxis MedStation ES (Med ES Main Tower)
- REF352
- Lot codes and dates
- Software v1.7.3
- REF/UDI-DI
323/10885403512667352/10885403512674
- Amount recalled
- 622
Where it was sold
Why it was recalled
Due to an automated dispensing cabinet software issue, when a medication single order contains more than one component and at least one is unavailable for a multi-item or combination order, the order may display as grayed out; alternate location tooltip will display "Server connection failed," not listing other area devices where unavailable item(s) may be found, which may lead to delayed therapy.
This product could cause temporary or reversible health problems — stop using it.
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