Lower risk Medical device recall · FDA · Published February 14, 2023

BD Pyxis MedStation ES AUX Tower REF 343 BD Pyxis " MedStation 4000 AUX Tower REF 314

CareFusion 303

Plain-English summary generated from official FDA data by GovInfoNow · Published by Carlos Caban · How we make summaries

🇺🇸 FDA recall #Z-1050-2025Medical device CareFusion 303 ›

Lower-risk recall

Due to an increase in complaints of door latch assembly failures that may cause the doors to be left in an open state potentially causing inventory discrepancies, a delay in access to medication and/or diversion of medication.

Take action

Contact the company

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

✎ GovInfoNow plain-language explainer

CareFusion 303 Read more at govinfonow.com/recall/58895-carefusion-303.

Source Summary by GovInfoNow · govinfonow.com/recall/58895-carefusion-303 · Updated August 19, 2026 · FDA enforcement record: FDA #Z-1050-2025

Cite this page

“BD Pyxis MedStation ES AUX Tower REF 343 BD Pyxis " MedStation 4000 AUX Tower REF 314.” GovInfoNow, updated August 19, 2026. https://govinfonow.com/recall/58895-carefusion-303. Based on FDA recall #Z-1050-2025 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1050-2025%22&limit=1).

The U.S. Food and Drug Administration (FDA) has issued a recall for certain medical devices manufactured by CareFusion 303, Inc. due to potential safety hazards.

How to tell if you have it

CareFusion 303, Inc.
U.S. Food and Drug Administration (FDA)

The hazard

The specific hazard details are not provided in the available text; however, previous recalls by this manufacturer have involved risks such as fingerprint scanner overheating causing burns, software issues preventing timely updates of patient information, and labeling errors regarding Transport Layer Security (TLS) versions for secure Wi-Fi communication.

Context

CareFusion 303, Inc. has a history of recalls since June 12, 2017. Recent related recalls include: BD Pyxis MedStation 403 Medication Cabinet (April 30, 2026) for overheating fingerprint scanners; CareFusion labeling issues regarding TLS versions (February 11, 2026); and BD Pyxis ES Enterprise Server Software Update Issue (December 3, 2025).

How to tell if you have this one

CareFusion 303

Brand
CareFusion 303
Category
Medical device

Based on the official FDA remedy

What to do — step by step

Check for updates
CareFusion 303
Update software
CareFusion 303

Where it went and when

Where it was distributed

Distributed in 50 states and D.C. and Puerto Rico, and outside the U.S.

FDA distribution: “U.S.: AK, AL, AR, AZ, CA, CO, CT, DC, DE, FL, GA, GU, HI, IA, ID, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MP, MS, MT, NC, ND, NE, NH, NJ, NM, NV, NY, OH, OK, OR, PA, PR, RI, SC, SD, TN, TX, UT, VA, VT, WA, WI, WV, and WY. O.U.S.:…” States read from FDA’s own wording; “not listed” means the notice does not name it.

States: Alabama, Alaska, Arizona, Arkansas, California, Colorado, Connecticut, Delaware, District of Columbia, Florida, Georgia, Hawaii, Idaho, Illinois, Indiana, Iowa, Kansas, Kentucky, Louisiana, Maine, Maryland, Massachusetts, Michigan, Minnesota, Mississippi, Missouri, Montana, Nebraska, Nevada, New Hampshire, New Jersey, New Mexico, New York, North Carolina, North Dakota, Ohio, Oklahoma, Oregon, Pennsylvania, Puerto Rico, Rhode Island, South Carolina, South Dakota, Tennessee, Texas, Utah, Vermont, Virginia, Washington, West Virginia, Wisconsin, Wyoming.

Recall timeline

FDA published this recall 2 years after the firm started it.

Feb 14, 2023Firm started the recall
Jan 30, 2025FDA classified it Class II
Feb 5, 2025Published in FDA’s Enforcement Report

Dates from the agency record only; steps without a date are left out.

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Link to this recall

<a href="https://govinfonow.com/recall/58895-carefusion-303">BD Pyxis MedStation ES AUX Tower REF 343 BD Pyxis " MedStation 4000 AUX Tower REF 314 (GovInfoNow)</a>

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-1050-2025 (February 14, 2023) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-1050-2025 to see it in context.
Plain-language summary written by qwen3:4b on August 19, 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.