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Lower risk Food recall · FDA · Published March 1, 2018

KUIYI Grilled Crispy Shrimp Recall: Nitrofurans Found in Product

KUIYI International recalls Grilled Crispy Shrimp (20g*20 and 16g*24) with UPC 6923006800082 due to nitrofurans detected. Consumers should check expiration date and stop using if concerned.

🇺🇸 FDA recall #F-1538-2018FoodKUIYI ›
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Recalling firmKUIYI INTERNATIONAL INC.17558 Rowland St · City Of Industry, CA 91748-1114
✎ GovInfoNow plain-language explainer

What happened, in plain English

KUIYI International is recalling Grilled Crispy Shrimp products (20g*20 and 16g*24) because they tested positive for nitrofurans. This chemical is a potential health risk, so affected consumers should stop using the product if they have it. Read more at govinfonow.com/recall/19608-kuiyi-grilled-crispy-shrimp-recall-nitrofurans-found-in-product.

Source Summary by GovInfoNow · govinfonow.com/recall/19608-kuiyi-grilled-crispy-shrimp-recall-nitrofurans-found-in-product · Updated October 7, 2026 · FDA enforcement record: FDA #F-1538-2018

Cite this page

“KUIYI Grilled Crispy Shrimp Recall: Nitrofurans Found in Product.” GovInfoNow, updated October 7, 2026. https://govinfonow.com/recall/19608-kuiyi-grilled-crispy-shrimp-recall-nitrofurans-found-in-product. Based on FDA recall #F-1538-2018 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-1538-2018%22&limit=1).

Why it’s dangerous

Nitrofurans are antibiotics that can be harmful when consumed in food. They are not supposed to be in food products and can cause health issues if ingested.

Who’s affected

Anyone who purchased KUIYI Grilled Crispy Shrimp (20g*20 and 16g*24) with UPC 6923006800082 before expiration date 10/09/2018. People with food allergies to nitrofurans may be at higher risk.

How to tell if you have this one

Check for the UPC code 6923006800082 on the packaging. The product was sold with an expiration date of 10/09/2018.

  • Brand
    KUIYI
  • Category
    Food
Based on the official FDA remedy

What to do — step by step

  1. Check Product Details

    Look for the UPC code 6923006800082 and expiration date 10/09/2018 on the packaging.

Where it went and when

Where it was distributed

Distributed in California.

Alaska: not listedAKMaine: not listedMEVermont: not listedVTNew Hampshire: not listedNHWashington: not listedWAIdaho: not listedIDMontana: not listedMTNorth Dakota: not listedNDMinnesota: not listedMNIllinois: 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: yesCAUtah: 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: not listedNCSouth Carolina: not listedSCDistrict of Columbia: not listedDCOklahoma: not listedOKLouisiana: not listedLAMississippi: not listedMSAlabama: not listedALGeorgia: not listedGAHawaii: not listedHITexas: not listedTXFlorida: not listedFL

FDA distribution: “U.S. distribution to CA. No foreign distribution.” States read from FDA’s own wording; “not listed” means the notice does not name it.

States: California.

Recall timeline

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

1. Firm started the recall: Mar 1, 201812. FDA classified it Class II: Jun 7, 201823. Published in FDA’s Enforcement Report: Jun 13, 201834. FDA terminated the recall: Aug 27, 201842018
  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-1538-2018 (March 1, 2018) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-1538-2018 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.
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