Reported Jun 5, 2024 · Ongoing
BD Pyxis MedStation ES, REF: 323, Medication Cabinet
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
- REF323, Medication Cabinet
- Lot codes and dates
- UDI10885403512667/New
- Serial Numbers reported 8/27/25
3,616 of 3,616 codes
148790211568338115683382156833851568338615683387156833881568338915683390156749881567499215674993156749941567499515674996156749981567499915675000156750011567503615758077157580781575807915755497157554991575550115754424172697621362568013625681136256821362568413611196136111981361120413467008133360111333601313336014133360151333601614386862142656291426563014202688142026891420269014202691142026921419483914194841141948421415720214157203141572041415720514157206141572071415720814157209
- Amount recalled
- 212,367 units
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
Why it was recalled
Potential fluid ingress of anesthesia station or med station may result in smoke, system downtime and/or fire.
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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