Mycotoxins in US Food Imports — FDA Import Refusals

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Mycotoxins appeared in 88 FDA import refusals between 2020 and 2026 — 0.3% of the 25,860 refusals that identify a hazard. The origins cited most often are El Salvador, India, Mexico. The most-affected product category is Nuts and Edible Seeds. Volume in 2025 was up 47% on 2024.

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Mycotoxins notifications by year

YearNotificationsof which border rejectionsYoY
2020 10 10
2021 11 11 +10.0%
2022 14 14 +27.3%
2023 8 8 -42.9%
2024 15 15 +87.5%
2025 22 22 +46.7%
2026 8 8 YTD
Total88

Origins most cited for Mycotoxins

#Origin countryNotifications
1 El Salvador 20
2 India 16
3 Mexico 10
4 United States 9
5 Turkey 8
6 Haiti 4
7 Afghanistan 3
8 Ghana 3
9 Hong Kong 3
10 Philippines 3
11 Argentina 2
12 Bangladesh 1
13 Canada 1
14 Germany 1
15 Indonesia 1
16 Nicaragua 1
17 Pakistan 1
18 Thailand 1

Product categories where Mycotoxins appears

#Product categoryNotifications
1Nuts and Edible Seeds34
2Whole Grains, Milled Grain Products, and Starch26
3Candy Without Chocolate, Candy Specialties, and Chewing Gum10
4Fruit and Fruit Products9
5Snack Food Items (Flour, Meal, or Vegetable Base)5
6Spices, Flavors, and Salts2
7Fishery/Seafood Products1
8Vegetables and Vegetable Products1

Recent Mycotoxins notifications

About Mycotoxins

Mycotoxin charges are brought under Section 402(a)(1): the food appears to bear or contain a poisonous and deleterious mould-produced toxin, most often aflatoxin, but also deoxynivalenol, fumonisin, ochratoxin A or patulin. These toxins form when crops are stored warm and damp rather than during processing, so the charge tracks growing and storage conditions in the country of origin as much as the product itself. Refusals concentrate in tree nuts, peanuts, dried figs, spices, corn and apple products such as juice, where the source mould thrives.

Which FDA import refusals does this page count?

Every entry FDA refused that cites this hazard among its charge codes. A single entry can carry more than one charge, so an entry refused for both a pathogen and a labelling defect is counted on both the relevant hazard page and, separately, in the hazard/paperwork split shown on the leaderboard.

What happens when this hazard is found in a shipment?

The entry is refused admission into US commerce. The importer must recondition the shipment (where that is possible), export it out of the United States, or have it destroyed under FDA supervision. Repeated findings against one shipper or product can lead FDA to place them on an Import Alert, which subjects future shipments to detention without physical examination.

Where does this data come from?

The public FDA Import Refusal Report, refetched weekly. Counts are per entry (consignment), so one entry listing several charge codes for the same hazard is counted once.