Simplot Exotic Grains Blend Recall: Undeclared Wheat Hazard
Simplot recalls 15-lb exotic grains blend due to undeclared wheat. This gluten-free product may contain wheat, posing a risk for those with celiac disease or gluten allergies.
Lower-risk recall
Simplot Good Grains Exotic Grains & Fire-Roasted Vegetable Blend is recalled due to undeclared wheat.
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What happened, in plain English
Simplot is recalling its Exotic Grains & Fire-Roasted Vegetable Blend because it contains undeclared wheat. This poses a risk for people with celiac disease or gluten allergies, as the product is labeled gluten-free but may have wheat. Read more at govinfonow.com/recall/18767-simplot-exotic-grains-blend-recall-undeclared-wheat-hazard.
Source Summary by GovInfoNow · govinfonow.com/recall/18767-simplot-exotic-grains-blend-recall-undeclared-wheat-hazard · Updated October 6, 2026 · FDA enforcement record: FDA #F-1844-2018
Cite this page
“Simplot Exotic Grains Blend Recall: Undeclared Wheat Hazard.” GovInfoNow, updated October 6, 2026. https://govinfonow.com/recall/18767-simplot-exotic-grains-blend-recall-undeclared-wheat-hazard. Based on FDA recall #F-1844-2018 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-1844-2018%22&limit=1).
Why it’s dangerous
The product is labeled gluten-free but contains undeclared wheat. This can cause health issues for individuals with celiac disease or gluten allergies who require strict wheat-free products.
Who’s affected
People with celiac disease or gluten allergies are at risk because the product is labeled gluten-free but contains undeclared wheat. The product is sold in frozen bags.
How to tell if you have this one
Check for the product name 'Exotic Grains & Fire-Roasted Vegetable Blend' with a 15-lb net weight. The UPC code is 1007117012948. The product is frozen and sold in 6 bags of 2.5 lbs each.
- Brand
Simplot- Category
Food
What to do — step by step
Check Product Label
Look for the label that states 'Gluten Free' but may contain undeclared wheat.
Where it went and when
Where it was distributed
Distributed in 16 states.
FDA distribution: “distributed in CA, CO, CT, FL, GA, KS, MD, MI, MT, NC, NV, NY, PA, VA, WA, and WI.” States read from FDA’s own wording; “not listed” means the notice does not name it.
States: California, Colorado, Connecticut, Florida, Georgia, Kansas, Maryland, Michigan, Montana, Nevada, New York, North Carolina, Pennsylvania, Virginia, Washington, Wisconsin.
Recall timeline
FDA terminated this recall 47 days 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-1844-2018 (August 3, 2018) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-1844-2018 to see it in context.
- Plain-language summary written by qwen3:4b on October 6, 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.