Cece's Veggie Co. Ramen with Listeria Contamination Risk
Veggie Noodle Co recalls Cece's Veggie Co. Fresh Veggie Ramen with Chicken Broth (11.5 oz) due to potential Listeria monocytogenes contamination. Consumers should avoid use.
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Potential to be contaminated with Listeria monocytogenes
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What happened, in plain English
Veggie Noodle Co is recalling Cece's Veggie Co. Fresh Veggie Ramen with Chicken Broth (11.5 oz) because it may be contaminated with Listeria monocytogenes. This bacteria can cause serious illness, so affected consumers should stop using the product. Read more at govinfonow.com/recall/16092-cece-s-veggie-co-ramen-with-listeria-contamination-risk.
Source Summary by GovInfoNow · govinfonow.com/recall/16092-cece-s-veggie-co-ramen-with-listeria-contamination-risk · Updated October 5, 2026 · FDA enforcement record: FDA #F-0509-2020
Cite this page
“Cece's Veggie Co. Ramen with Listeria Contamination Risk.” GovInfoNow, updated October 5, 2026. https://govinfonow.com/recall/16092-cece-s-veggie-co-ramen-with-listeria-contamination-risk. Based on FDA recall #F-0509-2020 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-0509-2020%22&limit=1).
Why it’s dangerous
Listeria monocytogenes is a bacteria that can cause serious infections, especially in pregnant women, newborns, and people with weakened immune systems. Contaminated food can lead to illness if eaten.
Who’s affected
Anyone who purchased Cece's Veggie Co. Fresh Veggie Ramen with Chicken Broth (11.5 oz) with UPC 5228700653. People with weakened immune systems are at higher risk for serious illness.
How to tell if you have this one
Check for the product name 'Cece's Veggie Co. Fresh Veggie Ramen with Chicken Broth (11.5 oz)' on the package. The UPC code is 5228700653. The product was sold from December 26, 2019, through January 8, 2020.
- Brand
Veggie Noodle Co- Product
Cece's Veggie Co. brand Fresh Veggie Ramen with Chicken Broth (11.5 oz, UPC 5228700653) packaged in a plastic tray- Category
Food
What to do — step by step
Stop Using Now
Discard the product immediately as it may be contaminated with Listeria monocytogenes.
Where it went and when
Where it was distributed
Distributed in 8 states.
FDA distribution: “TX, MN, GA, CA, CO, FL, MD, IL” States read from FDA’s own wording; “not listed” means the notice does not name it.
States: California, Colorado, Florida, Georgia, Illinois, Maryland, Minnesota, Texas.
Recall timeline
FDA terminated this recall 4 months after the firm started it.
- Firm started the recall
- FDA classified it Class I
- Published in FDA’s Enforcement Report
- FDA terminated the recall
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 #F-0509-2020 (December 26, 2019) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-0509-2020 to see it in context.
- Plain-language summary written by qwen3:4b on October 5, 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.