Fairview Mills Corn Flour Recall: Gluten Not Listed on Label
Fairview Mills recalls bulk food-grade pre-gel corn flour due to undetected gluten. The product does not list wheat on its label, posing a risk for gluten-sensitive individuals.
Lower-risk recall
Testing revealed the presence of gluten in the corn flour product. The corn flour product does not declare wheat on the label.
Contact the company
What happened, in plain English
Fairview Mills is recalling bulk food-grade pre-gel corn flour because testing found gluten present. This product does not list wheat on its label, which could be dangerous for people with gluten sensitivities or celiac disease. Read more at govinfonow.com/recall/18099-fairview-mills-corn-flour-recall-gluten-not-listed-on-label.
Source Summary by GovInfoNow · govinfonow.com/recall/18099-fairview-mills-corn-flour-recall-gluten-not-listed-on-label · Updated October 5, 2026 · FDA enforcement record: FDA #F-0631-2019
Cite this page
“Fairview Mills Corn Flour Recall: Gluten Not Listed on Label.” GovInfoNow, updated October 5, 2026. https://govinfonow.com/recall/18099-fairview-mills-corn-flour-recall-gluten-not-listed-on-label. Based on FDA recall #F-0631-2019 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-0631-2019%22&limit=1).
Why it’s dangerous
The corn flour contains gluten that is not listed on the label. This can cause health issues for individuals with gluten allergies or sensitivities, as the product is intended for use in food preparation.
Who’s affected
People who have purchased the recalled corn flour are at risk if they have gluten sensitivities or celiac disease. The product is sold in bulk and may be used in food preparation.
How to tell if you have this one
Check for the product code S100233-2018 or S100234-2018 on the packaging. The product is labeled as 'Food Grade Pre-Gel Corn Flour' and sold in bulk.
- Brand
Fairview Mills- Category
Food
What to do — step by step
Check Product Label
Look for the product codes S100233-2018 or S100234-2018 on the packaging.
Where it went and when
Where it was distributed
Distributed in Wisconsin.
FDA distribution: “One customer in Wisconsin.” States read from FDA’s own wording; “not listed” means the notice does not name it.
States: Wisconsin.
Recall timeline
FDA terminated this recall 4 months after the firm started it.
- Firm started the recall
- FDA classified it Class II
- 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-0631-2019 (November 2, 2018) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-0631-2019 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.