CareFusion BD Pyxis Pro MedStation Main Recall: Fluid Ingress Risk

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Contact the company & request your remedy

Recalling firmCareFusion 303, Inc.10020 Pacific Mesa Blvd, N/A · San Diego, CA 92121-4386

No email on file — write to the address above instead.

✎ GovInfoNow plain-language explainer

What happened, in plain English

CareFusion is recalling BD Pyxis Pro MedStation Main devices because fluid entering the system could cause smoke, system shutdowns, or fire. This affects medical devices used in healthcare settings.

Why it’s dangerous

Fluid ingress into the anesthesia station or med station could cause smoke, system downtime, or fire. This happens when the device is not properly sealed or maintained.

Who’s affected

Healthcare facilities using the BD Pyxis Pro MedStation Main device are most at risk. Patients and staff could be affected if the device malfunctions.

How to tell if you have this one

Check for the model number 'BD Pyxis Pro MedStation Main' and reference number '1155-00'. Affected units have specific serial numbers starting with 1155-00 10885403521300.

Brand
CareFusion
Category
Medical device

Based on the official FDA remedy

What to do — step by step

Check Device Serial Number
Look for the serial number on the device label, which starts with '1155-00 10885403521300'.

✎ GovInfoNow

Questions people ask

Is this device dangerous?

Yes, fluid ingress could cause smoke, system downtime, or fire.

What should I do if I have this device?

Check the serial number to see if it's affected. If so, contact CareFusion for instructions.

How can I tell if my device is recalled?

Look for the model 'BD Pyxis Pro MedStation Main' and reference number '1155-00' with the specific serial number starting with '1155-00 10885403521300'.

Take action

Contact CareFusion

We’ve drafted a message you can send CareFusion to request your refund or repair — edit it as you like.

✉️ Open in email

Subject: Recall Z-0370-2026 — CareFusion CareFusion

Hello,

I own a CareFusion that is covered by recall Z-0370-2026 from CareFusion.

I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this?

Thank you.

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Where this comes from

The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.

Official source: FDA Recall #Z-0370-2026 (September 30, 2025) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-0370-2026 to see it in context.
Plain-language summary written by qwen3:4b on August 17, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.

CareFusion 303, Inc. recalls BD Pyxis Pro MedStation Main, REF: 1155-00

Use caution until it’s fixed