FDA refusal charge AFLATOXIN: aflatoxin

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The AFLATOXIN charge appeared in 45 FDA import refusals between 2020 and 2026 — 0.2% of the 19,123 refusals that identify a hazard. The origins cited most often are El Salvador, Mexico, United States. The most-affected product category is Nuts and Edible Seeds. Volume in 2025 was up 12% on 2024.

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What FDA's charge says

AFLATOXIN is the code FDA prints on a refusal; below is the charge language FDA publishes for it, quoted from its charge table, with the sections of the FD&C Act it cites.

The article appears to contain a mycotoxin, a poisonous and deleterious substance which may render it injurious to health.

Sections 402(a)(1), 801(a)(3); ADULTERATION

AFLATOXIN refusals by year

YearRefusalsYoY
20208—
20213-62.5%
20226+100.0%
20234-33.3%
20248+100.0%
20259+12.5%
20267—YTD
Total45

Origins most often refused under AFLATOXIN

#Origin countryRefusals
1El Salvador8
2Mexico7
3United States7
4India6
5Turkey5
6Hong Kong3
7Haiti2
8Afghanistan1
9Bangladesh1
10Germany1
11Ghana1
12Nicaragua1
13Pakistan1
14Thailand1

Product categories refused under AFLATOXIN

#Product categoryRefusals
1Nuts and Edible Seeds22
2Whole Grains, Milled Grain Products, and Starch10
3Candy Without Chocolate, Candy Specialties, and Chewing Gum7
4Fruit and Fruit Products2
5Snack Food Items (Flour, Meal, or Vegetable Base)2
6Fishery/Seafood Products1
7Vegetables and Vegetable Products1

Latest refusals citing AFLATOXIN

About AFLATOXIN

What does the FDA import refusal charge AFLATOXIN mean?

FDA uses AFLATOXIN for: aflatoxin. Its published charge language reads: “The article appears to contain a mycotoxin, a poisonous and deleterious substance which may render it injurious to health.”

Is AFLATOXIN a food safety finding?

Yes. This site counts AFLATOXIN as a hazard finding, so a refusal citing it is on the hazard side of the hazard and paperwork split, whatever else the refusal cites.

What happens to a shipment refused under AFLATOXIN?

Under section 801(a) of the FD&C Act a refused entry has to be exported or destroyed, normally within 90 days of the notice of refusal. Bringing a product into compliance, for instance by relabelling, is something the importer asks FDA for before the decision is final. The notice itself and FDA's guidance govern a particular case; this page describes the published data and is not legal advice.