Reported Feb 19, 2025 · Ongoing
(1) Pyxis MedStation ES, Catalog No. 323; (2) Pyxis Anesthesia Station (PAS), Catalog No. 327; (3) Pyxis MedStation ES…
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?
(1) Pyxis MedStation ESCatalog No. 323(2) Pyxis Anesthesia Station (PAS)Catalog No. 327(3) Pyxis MedStation ES TowerCatalog No. 352(4) BD Pyxis CII Safe ESCatalog No. 1116-00
- Lot codes and dates
6 of 6 products
Products covered by this recall Model / number Barcodes Product as published 32310885403512667(1) Pyxis MedStation ES, , UDI-DI 10885403512667 32710885403477836(2) Pyxis Anesthesia Station (PAS), , UDI-DI 10885403477836 35210885403512674(3) Pyxis MedStation ES Tower, , UDI-DI 10885403512674 1116-0010885403512605(4) BD Pyxis CII Safe ES, , UDI-DI 10885403512605 — All Serial Numbers — Software Versions v1.10 and prior Affected - Amount recalled
- 137,741 total
This recall covers 6 products
The agency filed one notice per product. You are reading one of them; the other 5 are below.
Where it was sold
- Nationwide
Why it was recalled
Software issues could potentially result in: 1) delays in accessing dispensing software application, 2) wrong therapy (dose, item, timing, etc.), or 3) unauthorized access and/or compliance related issues
This product could cause temporary or reversible health problems — stop using it.
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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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