FDA refusal charge FOREIGN OB: foreign object

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The FOREIGN OB charge appeared in 57 FDA import refusals between 2020 and 2025 — 0.3% of the 19,123 refusals that identify a hazard. The origins cited most often are India, China, Japan. The most-affected product category is Spices, Flavors, and Salts. Volume in 2025 was up 67% on 2024.

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What FDA's charge says

FOREIGN OB 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 consist in whole or in part of a filthy, putrid, or decomposed substance, or is otherwise unfit for food in that it appears to contain foreign objects.

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

FOREIGN OB refusals by year

YearRefusalsYoY
20209—
202118+100.0%
202215-16.7%
20237-53.3%
20243-57.1%
20255+66.7%
Total57

Origins most often refused under FOREIGN OB

#Origin countryRefusals
1India37
2China5
3Japan4
4-3
5Mexico2
6Taiwan2
7Armenia1
8Italy1
9Tanzania1
10United States1

Product categories refused under FOREIGN OB

#Product categoryRefusals
1Spices, Flavors, and Salts32
2Candy Without Chocolate, Candy Specialties, and Chewing Gum11
3Fruit and Fruit Products8
4Vegetables and Vegetable Products2
5Chocolate and Cocoa Products1
6Fishery/Seafood Products1
7Gelatin, Rennet, Pudding Mixes, and Pie Fillings1
8Nuts and Edible Seeds1

Latest refusals citing FOREIGN OB

About FOREIGN OB

What does the FDA import refusal charge FOREIGN OB mean?

FDA uses FOREIGN OB for: foreign object. Its published charge language reads: “The article appears to consist in whole or in part of a filthy, putrid, or decomposed substance, or is otherwise unfit for food in that it appears to contain foreign objects.”

Is FOREIGN OB a food safety finding?

Yes. This site counts FOREIGN OB 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 FOREIGN OB?

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.