Siam Trading Khaotan Rice Cracker Recall: Undeclared Cashews
Siam Trading Inc. recalls Khaotan Rice Cracker (150g) due to undeclared cashews. Consumers should check product codes or best by dates for affected items.
Lower-risk recall
Mae Bua Jun/Khaotan Rice Cracker contains visible cashews that are not declared.
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What happened, in plain English
Siam Trading Inc. is recalling Khaotan Rice Cracker (150g) because it contains visible cashews that aren't listed on the label. This could mislead consumers about the product's ingredients, but it doesn't pose a direct health risk. Read more at govinfonow.com/recall/15507-siam-trading-khaotan-rice-cracker-recall-undeclared-cashews.
Source Summary by GovInfoNow · govinfonow.com/recall/15507-siam-trading-khaotan-rice-cracker-recall-undeclared-cashews · Updated October 5, 2026 · FDA enforcement record: FDA #F-1144-2020
Cite this page
“Siam Trading Khaotan Rice Cracker Recall: Undeclared Cashews.” GovInfoNow, updated October 5, 2026. https://govinfonow.com/recall/15507-siam-trading-khaotan-rice-cracker-recall-undeclared-cashews. Based on FDA recall #F-1144-2020 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-1144-2020%22&limit=1).
Why it’s dangerous
The rice cracker contains visible cashews that aren't declared on the label. This means consumers might not know they're eating cashews, which could be a problem for people with nut allergies or dietary restrictions. However, the cashews themselves aren't harmful in normal use.
Who’s affected
Anyone who purchased the Khaotan Rice Cracker (150g) from stores or online. People most at risk are those who rely on accurate ingredient labeling for dietary reasons.
How to tell if you have this one
Check the product for the brand 'Siam Trading' and product code or best by date. The item is sold in 150g packages.
- Brand
Siam Trading- Category
Food
What to do — step by step
Check Product Details
Look for the product code or best by date on the Khaotan Rice Cracker (150g) package.
Where it went and when
Where it was distributed
Distributed in 11 states.
FDA distribution: “NY, VA, NC, OH, IN, WI, MN, IL, PA, IA, NE” States read from FDA’s own wording; “not listed” means the notice does not name it.
States: Illinois, Indiana, Iowa, Minnesota, Nebraska, New York, North Carolina, Ohio, Pennsylvania, Virginia, Wisconsin.
Recall timeline
FDA terminated this recall 6 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-1144-2020 (July 13, 2020) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-1144-2020 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.