Import Alert

Breaking Trade News: American Producers of Aluminum Extrusions File Trade Petitions Alleging Unfair Dumping and Subsidies from 15 Countries

The U.S. Aluminum Extruders Coalition and the United Steelworkers (USW) union filed petitions claiming unfair trading imports of aluminum extrusions from China, Colombia, the Dominican Republic, Ecuador, India, Indonesia, Italy, Malaysia, Mexico, South Korea, Taiwan, Thailand, Turkey, the United Arab Emirates, and Vietnam.

Full list of exporters here, full list of U.S. importers here.

The filing is in response to increasing volumes of allegedly unfairly priced imports of aluminum extrusions that have been growing since 2019, notwithstanding that Aluminum Extrusions made in the U.S. face significantly higher costs due to restrictions on the importation of primary aluminum.

The petitions aim to demonstrate that aluminum extrusion producers in these countries are selling extrusions in the U.S. at less than fair value and that such sales are harming the U.S. Aluminum Extrusion industry. The petitions note dumped rates up to 256%.

The petitions also claims that producers in China, Indonesia, Mexico, and Turkey unfairly benefit from countervailable subsidies, such as tax breaks and discounted land.

The President of the Aluminum Extruders Council, Jeff Henderson, stated:  “For years, American extruders and workers have lost huge amounts of sales to unfairly traded, dumped and subsidized imports of aluminum extrusions. It’s time to take a stand for American manufacturing and take on these illegally traded products.”

The Commerce Department will determine whether to initiate the investigations within 20 days. The USITC will reach a preliminary determination of material injury or threat of material injury within 45 days. The deposit of duties will likely be required by the late fall […]

By |2023-10-06T13:59:01-04:00October 6, 2023|Import, Investigation|0 Comments

Don’t be a Target, Learn Best Practices to Mitigate FDA Enforcement

The U.S. Food and Drug Administration (FDA) is in full enforcement mode issuing 260 warning letters in 2021 alone! Now is the time to ensure your products are in compliance with the Federal Food, Drug, and Cosmetic Act (the Act) prior to importation. Manufacturers, importers, distributors, and others engaged in the production or sale of over the counter (OTC) drugs or cosmetic products must be aware of FDA’s various enforcement mechanisms, and more importantly,  how to avoid and/or mitigate such actions.  FDA’s most common enforcement activities include notices of FDA action, warning letters, seizures, voluntary recalls, injunctions, and criminal prosecution.



The Food Safety Modernization Act (“FSMA”) is in full force and the U.S. Food and Drug Association (FDA) is now enforcing its Foreign Supplier Verification Program (FSVP) regulation. This blog discusses FDA’s first FSVP Warning Letter and illustrates what NOT to do when FDA starts asking questions about your products. The FSVP regulation requires that importers perform certain risk-based activities to verify that human and/or animal food imported into the United States has been produced in a manner that meets applicable U.S. food safety standards.

In the case of the U.S. importer who received the FSVP Warning Letter, their FDA issues started in the beginning of 2019 when a salmonella outbreak ravished multiple states and was traced back to their Tahini product.


Here’s a Recap of Part II of our #WorldTradeMonth Seminar Series for Compliance Professionals on FDA FSMA and FSVP

Yesterday, we at DTL, had the pleasure of hosting Part II of our #WorldTradeMonth Seminar Series for Compliance Professionals. The second seminar focused on FDA FSMA (Food Safety Modernization Act) Compliance for Importers with expert speakers from the U.S. Food and Drug Administration (FDA) and industry. We had a packed house with an array of attendees such as importers of food, beverages, and medical devices, along with customs brokers, freight forwarders / NVOCCs, lawyers, consultants, and others. We received requests for a re-cap from those who attended and industry members who were not able to attend. You asked and we deliver. Here is our recap:



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