Adulteration violations continue to cause the most refusals of FDA-inspected food imports

Pir charts showing share of FDA refusals, by type of violations

The U.S. Food and Drug Administration (FDA) is responsible for overseeing the safety of most food sold in the United States, including food imported from other countries. A recent ERS study examined patterns in FDA import refusals over 2005-13 and compared results with an earlier study of data from 1998-2004. In both time periods, the majority of violations were for adulteration—problems relating to poisonous ingredients, disease-causing bacteria and viruses (pathogens), unsafe color additives, pesticide residues, or filth (visually apparent non-food material). Two product groups—fishery/seafood products and spices/flavors/salts—were responsible for the majority of violations for Salmonella bacteria. Chemical adulteration, including pesticide residues, accounted for a slightly larger share of import refusals in 2005-13. Chemical adulteration is a common type of adulteration violation in fresh produce and fruit and vegetable products. Misbranding violations for false, misleading, or missing labels accounted for 41 percent of violations in 2005-13, up from 33 percent in 1998-2004. The data for this chart come from the ERS report, FDA Refusals of Imported Food Products by Country and Category, 2005–2013, released on March 28, 2016.

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