Food and Drug Administration import alerts affecting the following have been newly issued or modified in the past week.

- animal dental spray from Sweden

- bath soaps from Germany

- beets from Mexico

- black fungus from China

- dates from Algeria

- dietary supplements from Mexico

- dried pollack from Korea

- frog legs from China

- ground corn from Nicaragua

- hard candy from India

- limes from Peru

- mascara from China

- massagers from Korea

- medical instruments from Pakistan

- milk with added multivitamins from Mexico

- mouthwash from India

- pepper soup powder from Nigeria

- sesame seeds from India

- shrimp from China and India

- snack mixes from Pakistan

- soft drinks from Guatemala

- surgical sutures from Korea

- vaping devices from China

- vitamins from Canada

Import alerts inform FDA field staff that the agency has enough evidence or other information to allow a product that appears to be in violation of FDA laws and regulations to be detained without physical examination at the time of entry. Import alerts may cover products from designated countries or areas (including from all foreign countries), manufacturers, or shippers.

Firms and/or products on the “red list” of an import alert are subject to DWPE, while firms and/or products on the “green list” are not because they have met the criteria for exclusion. Some import alerts include a “yellow list” of firms, products, and/or countries subject to intensified surveillance because the nature of the violations may warrant further field examinations of individual entries and/or additional analyses. In addition, depending on the specific import alert, shipments of products subject to DWPE may still be imported into the U.S. if the importer has demonstrated that the shipment is in compliance.

If a product is detained without physical examination the importer has the right to provide evidence to the FDA in an attempt to overcome the appearance of the violation. If no such evidence is submitted, or if the evidence provided is insufficient, the product will be subject to refusal of entry into the U.S.

For more information on this and other FDA issues, please contact FDA consultant Domenic Veneziano at (202) 734-3939 or via email.

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