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Lower risk Medical device recall · FDA · Published February 11, 2026

CareFusion 303, Inc. - CareFusion

CareFusion 303, Inc. is a company that produces medical devices and equipment. They are known for their innovative solutions in the healthcare industry.

🇺🇸 FDA recall #Z-1645-2026Medical deviceCareFusion 303, Inc. ›
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Contact the company

Recalling firmCareFusion 303, Inc.10020 Pacific Mesa Blvd · San Diego, CA 92121-4386
✎ GovInfoNow plain-language explainer

What happened, in plain English

CareFusion 303, Inc. is a company that produces medical devices and equipment. They are known for their innovative solutions in the healthcare industry. Read more at govinfonow.com/recall/50018-carefusion-303-inc-carefusion.

Source Summary by GovInfoNow · govinfonow.com/recall/50018-carefusion-303-inc-carefusion · Updated August 10, 2026 · FDA enforcement record: FDA #Z-1645-2026

Cite this page

“CareFusion 303, Inc. - CareFusion.” GovInfoNow, updated August 10, 2026. https://govinfonow.com/recall/50018-carefusion-303-inc-carefusion. Based on FDA recall #Z-1645-2026 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1645-2026%22&limit=1).

Why it’s dangerous

CareFusion 303, Inc. is a legitimate company that produces medical devices and equipment. They are known for their innovative solutions in the healthcare industry. There is no evidence of malicious activity or data breaches associated with this company.

Who’s affected

All users of CareFusion 303, Inc. products

How to tell if you have this one

Check for the company's official website and product documentation to ensure you are using legitimate products. Look for security updates and patches from the manufacturer.

  • Brand
    CareFusion 303, Inc.
  • Category
    Medical device
Based on the official FDA remedy

What to do — step by step

  1. 1

    Verify the company's legitimacy by checking their official website and product documentation.

  2. 2

    Ensure you are using the latest version of the product and any available security updates.

  3. 3

    Report any suspicious activity or security concerns to the company's customer support.

Where it went and when

Where it was distributed

Distributed nationwide and abroad; the notice names 49 states.

Alaska: nationwideAKMaine: named in the noticeMEVermont: named in the noticeVTNew Hampshire: named in the noticeNHWashington: named in the noticeWAIdaho: named in the noticeIDMontana: named in the noticeMTNorth Dakota: named in the noticeNDMinnesota: named in the noticeMNIllinois: named in the noticeILWisconsin: named in the noticeWIMichigan: named in the noticeMINew York: named in the noticeNYRhode Island: named in the noticeRIMassachusetts: named in the noticeMAOregon: named in the noticeORNevada: named in the noticeNVWyoming: named in the noticeWYSouth Dakota: named in the noticeSDIowa: named in the noticeIAIndiana: named in the noticeINOhio: named in the noticeOHPennsylvania: named in the noticePANew Jersey: named in the noticeNJConnecticut: named in the noticeCTCalifornia: named in the noticeCAUtah: named in the noticeUTColorado: named in the noticeCONebraska: named in the noticeNEMissouri: named in the noticeMOKentucky: named in the noticeKYWest Virginia: named in the noticeWVVirginia: named in the noticeVAMaryland: named in the noticeMDDelaware: named in the noticeDEArizona: named in the noticeAZNew Mexico: named in the noticeNMKansas: named in the noticeKSArkansas: named in the noticeARTennessee: named in the noticeTNNorth Carolina: named in the noticeNCSouth Carolina: named in the noticeSCDistrict of Columbia: named in the noticeDCOklahoma: named in the noticeOKLouisiana: named in the noticeLAMississippi: named in the noticeMSAlabama: named in the noticeALGeorgia: named in the noticeGAHawaii: named in the noticeHITexas: named in the noticeTXFlorida: named in the noticeFLPuerto Rico: named in the noticePR

FDA distribution: “Worldwide distribution: U.S.(Nationwide) to states of: 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,…” States read from FDA’s own wording; “not listed” means the notice does not name it.

Named in the notice: Alabama, 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 49 days after the firm started it.

1. Firm started the recall: Feb 11, 202612. FDA classified it Class II: Mar 26, 202623. Published in FDA’s Enforcement Report: Apr 1, 202632026
  1. Firm started the recall
  2. FDA classified it Class II
  3. Published in FDA’s Enforcement Report

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

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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-1645-2026 (February 11, 2026) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-1645-2026 to see it in context.
  • Plain-language summary written by qwen3:4b on August 10, 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.