Reported Jun 5, 2024 · Ongoing
BD Pyxis(TM) Anesthesia Station 4000, REF: 338
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(TM) Anesthesia Station 4000
- REF338
- Lot codes and dates
- UDI10885403477829/
- Serial Numbers provided 8/27/2025
3,616 of 3,616 codes
155492571489766314895303148953041489530514895306148953071489530814895309148953101489531114877974148196961495642514956427149564281495642914956431149564321462288414622885150917201454646914361326143613271501961115019612150196131501961415019615150196161501961715019618150196191501962015289651145585941455859514558596145585971455859814558599145586001455860114558602145586041455860514558606145586071438423414384236143842381438424014384241143842431438424414384245143842461438424714384248
- Amount recalled
- 11,875 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.
Want the full recall guide?
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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