General Mills IQF White Rice ES CA Recall: Contains Eggs and Wheat
General Mills recalls IQF White Rice ES CA (product #4621686100) due to potential egg and wheat contamination. Consumers should check packaging for the specific product code.
Lower-risk recall
General Mills was notified by customer of IQF noodles found in IQF rice. The IQF noodles contain eggs and wheat.
Contact the company
What happened, in plain English
General Mills is recalling IQF White Rice ES CA (product #4621686100) because it may contain eggs and wheat. This could be a problem for people with allergies to those ingredients. Read more at govinfonow.com/recall/20658-general-mills-iqf-white-rice-es-ca-recall-contains-eggs.
Source Summary by GovInfoNow · govinfonow.com/recall/20658-general-mills-iqf-white-rice-es-ca-recall-contains-eggs · Updated October 7, 2026 · FDA enforcement record: FDA #F-3336-2017
Cite this page
“General Mills IQF White Rice ES CA Recall: Contains Eggs and Wheat.” GovInfoNow, updated October 7, 2026. https://govinfonow.com/recall/20658-general-mills-iqf-white-rice-es-ca-recall-contains-eggs. Based on FDA recall #F-3336-2017 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-3336-2017%22&limit=1).
Why it’s dangerous
The rice product contains eggs and wheat, which could cause allergic reactions in sensitive individuals. This is a food safety issue for those with allergies to these ingredients.
Who’s affected
People with egg or wheat allergies who consume the recalled rice may be at risk. The recall affects consumers who bought the specific product code.
How to tell if you have this one
Check for the product code 4621686100 on the cardboard tote. The recall applies to IQF White Rice ES CA sold in the United States.
- Brand
General Mills- Category
Food
What to do — step by step
Check Product Code
Look for the product code 4621686100 on the cardboard tote to confirm if the item is recalled.
Where it went and when
Where it was distributed
Distributed in Arkansas.
FDA distribution: “AR” States read from FDA’s own wording; “not listed” means the notice does not name it.
States: Arkansas.
Recall timeline
FDA terminated this recall 9 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-3336-2017 (July 19, 2017) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-3336-2017 to see it in context.
- Plain-language summary written by qwen3:4b on October 7, 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.