CareFusion 303, Inc. - Product List
CareFusion 303, Inc. is a company that produces medical devices and products. This page lists their product catalog.
Lower-risk recall
Due to customer complaints related to the MedBank software which may indicate that a different medication is loaded in a cubie (drawer) pocket than what is physically loaded and listed on the pocket label. As a result of this issue, a patient could receive the wrong medication or wrong dose of medication that could lead to patient harm.
Contact the company
What happened, in plain English
CareFusion 303, Inc. is a company that produces medical devices and products. This page lists their product catalog. Read more at govinfonow.com/recall/59172-carefusion-303-inc-product-list.
Source Summary by GovInfoNow · govinfonow.com/recall/59172-carefusion-303-inc-product-list · Updated August 19, 2026 · FDA enforcement record: FDA #Z-0928-2023
Cite this page
“CareFusion 303, Inc. - Product List.” GovInfoNow, updated August 19, 2026. https://govinfonow.com/recall/59172-carefusion-303-inc-product-list. Based on FDA recall #Z-0928-2023 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0928-2023%22&limit=1).
Why it’s dangerous
This page lists the product catalog of CareFusion 303, Inc. which is a medical device company. The products listed are medical devices that may be used in healthcare settings. The risk level is low because the products are for medical use and not for malicious purposes.
Who’s affected
All users of CareFusion 303, Inc. products
How to tell if you have this one
The product catalog of CareFusion 303, Inc. includes medical devices such as syringes, needles, and other medical equipment.
- Brand
CareFusion 303, Inc.- Category
Medical device
What to do — step by step
A
Ensure that all medical devices are used in accordance with the manufacturer's instructions.
B
Regularly check for updates to the product catalog to ensure that you have the latest information on available products.
C
If you are a healthcare professional, ensure that you are using the correct medical devices for your patient's needs.
Where it went and when
Where it was distributed
Distributed nationwide; the notice names 40 states.
FDA distribution: “U.S. Nationwide distribution including in the states of AK, AL, AZ, CA, CO, CT, FL, GA, IA, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MS, MT, NC, NE, NJ, NM, NV, NY, OH, OK, OR, PA, SC, SD, TN, TX, UT, WA, WI, and WV.” States read from FDA’s own wording; “not listed” means the notice does not name it.
Named in the notice: Alabama, Alaska, Arizona, California, Colorado, Connecticut, Florida, Georgia, Illinois, Indiana, Iowa, Kansas, Kentucky, Louisiana, Maine, Maryland, Massachusetts, Michigan, Minnesota, Mississippi, Missouri, Montana, Nebraska, Nevada, New Jersey, New Mexico, New York, North Carolina, Ohio, Oklahoma, Oregon, Pennsylvania, South Carolina, South Dakota, Tennessee, Texas, Utah, Washington, West Virginia, Wisconsin.
Recall timeline
FDA published this recall 37 days after the firm started it.
- Firm started the recall
- FDA classified it Class II
- Published in FDA’s Enforcement Report
Dates from the agency record only; steps without a date are left out.
Questions people ask
Are these products safe for use?
Yes, these products are designed and tested to meet medical safety standards.
How can I ensure I am using the correct product?
Always follow the manufacturer's instructions and consult with a healthcare professional if you are unsure.
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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-0928-2023 (December 12, 2022) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-0928-2023 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.