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Stop using now Food recall · FDA · Published July 3, 2017

HY-TOP Chicken Rice Recall: Undeclared Wheat Hazard

Trinidad Benham Corp recalls HY-TOP Chicken Flavored Rice & Vermicelli due to undeclared wheat. Check your pantry for affected lots.

🇺🇸 FDA recall #F-2948-2017FoodHY-TOP ›
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Contact the company

Recalling firmTrinidad Benham Corp3650 S Yosemite St · Denver, CO 80237-1800
✎ GovInfoNow plain-language explainer

What happened, in plain English

Trinidad Benham Corp is recalling HY-TOP Chicken Flavored Rice & Vermicelli with Seasonings because the product failed to declare wheat in its ingredient statement. This omission poses a risk to individuals with wheat allergies or celiac disease who may unknowingly consume an allergen. The recall covers specific lots distributed to Minnesota, North Carolina, and Texas. Read more at govinfonow.com/recall/20684-hy-top-chicken-rice-recall-undeclared-wheat-hazard.

Source Summary by GovInfoNow · govinfonow.com/recall/20684-hy-top-chicken-rice-recall-undeclared-wheat-hazard · Updated October 11, 2026 · FDA enforcement record: FDA #F-2948-2017

Cite this page

“HY-TOP Chicken Rice Recall: Undeclared Wheat Hazard.” GovInfoNow, updated October 11, 2026. https://govinfonow.com/recall/20684-hy-top-chicken-rice-recall-undeclared-wheat-hazard. Based on FDA recall #F-2948-2017 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-2948-2017%22&limit=1).

Why it’s dangerous

The product contains wheat, but it was not listed on the label. People with wheat allergies or celiac disease rely on ingredient labels to avoid triggers; consuming this undeclared allergen can cause serious allergic reactions or gastrointestinal distress.

Who’s affected

Consumers in Minnesota, North Carolina, and Texas who purchased the recalled rice mix are affected. Individuals with wheat allergies or celiac disease are at the highest risk of an allergic reaction or adverse health effect.

How to tell if you have this one

Check your pantry for HY-TOP Chicken Flavored Rice & Vermicelli with Seasonings in a 6.9 oz (196g) box. Verify the lot codes printed on the package: 14MAR18L, 18APR18L, 14MAY18L, or 15JUN18L.

  • Brand
    HY-TOP
  • Category
    Food
Based on the official FDA remedy

What to do — step by step

  1. Stop consuming the product

    Do not eat the recalled rice mix if you have a wheat allergy or celiac disease.

  2. Check your lot codes

    Verify if your box has one of the affected lot codes: 14MAR18L, 18APR18L, 14MAY18L, or 15JUN18L.

  3. Dispose of the product

    Throw away the recalled items to prevent accidental consumption by others in your household.

Where it went and when

Where it was distributed

Distributed in 3 states.

Alaska: not listedAKMaine: not listedMEVermont: not listedVTNew Hampshire: not listedNHWashington: not listedWAIdaho: not listedIDMontana: not listedMTNorth Dakota: not listedNDMinnesota: yesMNIllinois: not listedILWisconsin: not listedWIMichigan: not listedMINew York: not listedNYRhode Island: not listedRIMassachusetts: not listedMAOregon: not listedORNevada: not listedNVWyoming: not listedWYSouth Dakota: not listedSDIowa: not listedIAIndiana: not listedINOhio: not listedOHPennsylvania: not listedPANew Jersey: not listedNJConnecticut: not listedCTCalifornia: not listedCAUtah: not listedUTColorado: not listedCONebraska: not listedNEMissouri: not listedMOKentucky: not listedKYWest Virginia: not listedWVVirginia: not listedVAMaryland: not listedMDDelaware: not listedDEArizona: not listedAZNew Mexico: not listedNMKansas: not listedKSArkansas: not listedARTennessee: not listedTNNorth Carolina: yesNCSouth Carolina: not listedSCDistrict of Columbia: not listedDCOklahoma: not listedOKLouisiana: not listedLAMississippi: not listedMSAlabama: not listedALGeorgia: not listedGAHawaii: not listedHITexas: yesTXFlorida: not listedFL

FDA distribution: “Product was shipped to the following states: MN, NC & TX” States read from FDA’s own wording; “not listed” means the notice does not name it.

States: Minnesota, North Carolina, Texas.

Recall timeline

FDA terminated this recall 6 months after the firm started it.

1. Firm started the recall: Jul 3, 201712. FDA classified it Class II: Jul 27, 201723. Published in FDA’s Enforcement Report: Aug 2, 201734. FDA terminated the recall: Dec 18, 201742017
  1. Firm started the recall
  2. FDA classified it Class II
  3. Published in FDA’s Enforcement Report
  4. 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-2948-2017 (July 3, 2017) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-2948-2017 to see it in context.
  • Plain-language summary written by qwen3.6:35b-a3b on October 11, 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.
GovInfoNow is an independent guide. We are not FDA or any government agency. Always confirm details with the official recall.Data: CPSC · FDA · NHTSA · USDA