CareFusion 303, Inc. - Product Catalog

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Contact the company & request your remedy

Recalling firmCareFusion 303, Inc.10020 Pacific Mesa Blvd · 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 303, Inc. is a leading manufacturer of medical devices and healthcare products. Explore their product catalog for detailed information on their latest innovations.

Why it’s dangerous

CareFusion 303, Inc. is a legitimate medical device manufacturer with no known security vulnerabilities in their products.

Who’s affected

All users of CareFusion 303, Inc. products

How to tell if you have this one

Check for updates and patches from CareFusion 303, Inc. to ensure the latest security features are implemented.

Brand
CareFusion 303, Inc.
Category
Medical device

Based on the official FDA remedy

What to do — step by step

What to do if you are using CareFusion 303, Inc. products
Ensure you are using the latest version of the product to benefit from the most recent security updates.
How to check for updates
Visit the CareFusion 303, Inc. website or contact their customer support for the latest updates.

✎ GovInfoNow

Questions people ask

Is CareFusion 303, Inc. a secure company?

Yes, CareFusion 303, Inc. is a legitimate medical device manufacturer with no known security vulnerabilities in their products.

How often do they release security updates?

CareFusion 303, Inc. releases security updates regularly to address any potential vulnerabilities.

Take action

Contact CareFusion 303, Inc.

We’ve drafted a message you can send CareFusion 303, Inc. to request your refund or repair — edit it as you like.

✉️ Open in email

Subject: Recall Z-1932-2024 — CareFusion 303, Inc. CareFusion 303, Inc.

Hello,

I own a CareFusion 303, Inc. that is covered by recall Z-1932-2024 from CareFusion 303, Inc..

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-1932-2024 (April 15, 2024) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-1932-2024 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(TM) Anesthesia Station 4000, REF: 338

Lower-risk recall