Other pathogens in US Food Imports — FDA Import Refusals

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Other pathogens appeared in 33 FDA import refusals between 2020 and 2026 — 0.1% of the 25,860 refusals that identify a hazard. The origins cited most often are Philippines, India, Mexico. The most-affected product category is Vitamins, Minerals, Proteins, and Unconventional Dietary Specialties for Humans. Volume in 2025 was down 50% on 2024.

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Other pathogens notifications by year

YearNotificationsof which border rejectionsYoY
2020 7 7
2021 6 6 -14.3%
2022 8 8 +33.3%
2023 3 3 -62.5%
2024 4 4 +33.3%
2025 2 2 -50.0%
2026 3 3 YTD
Total33

Origins most cited for Other pathogens

#Origin countryNotifications
1 Philippines 8
2 India 7
3 Mexico 5
4 Nicaragua 3
5 El Salvador 2
6 Israel 2
7 United States 2
8 Canada 1
9 Chile 1
10 Indonesia 1
11 Russia 1

Product categories where Other pathogens appears

#Product categoryNotifications
1Vitamins, Minerals, Proteins, and Unconventional Dietary Specialties for Humans12
2Nuts and Edible Seeds7
3Cheese and Cheese Products6
4Fruit and Fruit Products3
5Fishery/Seafood Products1
6Milk, Butter, and Dried Milk Products1
7Multiple Food Dinners, Gravies, Sauces, and Specialties (Total Diet)1
8Spices, Flavors, and Salts1
9Vegetables and Vegetable Products1

Recent Other pathogens notifications

About Other pathogens

This group covers the remaining pathogens charged as poisonous or deleterious substances under Section 402(a)(1): E. coli O157:H7 and other Shiga toxin–producing strains, Shigella, Vibrio cholerae, Hepatitis A virus, and generic bacterial-contamination findings that do not name Salmonella or Listeria specifically. Each is grounds for refusal on its own, without a numeric threshold, because federal law treats their presence as adulteration outright. Refusals span produce, shellfish, spices and other foods where fecal or waterborne contamination can enter before or during processing.

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.