CareFusion 303, Inc. - Product Catalog

Take action

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 our comprehensive product catalog for the latest innovations in medical technology.

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 find a vulnerability
Report any vulnerabilities to CareFusion 303, Inc. through their official security channels.
How to verify product legitimacy
Check the product's official website or contact CareFusion 303, Inc. directly for verification.

✎ GovInfoNow

Questions people ask

Is CareFusion 303, Inc. a legitimate company?

Yes, CareFusion 303, Inc. is a legitimate medical device manufacturer with a long history of providing safe and reliable healthcare products.

How can I report a security vulnerability?

You can report vulnerabilities to CareFusion 303, Inc. through their official security contact information on their website.

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-0671-2025 — CareFusion 303, Inc. CareFusion 303, Inc.

Hello,

I own a CareFusion 303, Inc. that is covered by recall Z-0671-2025 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.

Similar recalls

From people who’ve dealt with this

Experiences, tips, and questions from readers. Every comment is reviewed before it appears.

No comments yet — be the first to share your experience.

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-0671-2025 (November 14, 2024) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-0671-2025 to see it in context.
Plain-language summary written by qwen3:4b on August 18, 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 MedStation ES 7 Drawer Auxiliary Tower, REF: 324

Lower-risk recall