Trade rule changes, 7 Sep to 13 Sep 2026

Last call: Final Hours Before the ACE User Satisfaction Survey Closes

CBP's 2026 ACE User Satisfaction Survey, open to all ACE trade community users, closes at 11:59 p.m. ET on September 11, 2026.

Modifying Section 338 Additional Duties on Certain Goods of Canada

CSMS #69851916 explains modifications to Section 338 additional duties on certain goods of Canada under a Presidential Proclamation issued September 8, 2026, affecting alcoholic beverages and motor vehicles.

United States surtax remission order (2025)

Ottawa, April 17, 2025 Updated: September 11, 2026 1.

Commission Implementing Decision (EU) 2026/2032 of 11 September 2026 amending Implementing Decision (EU) 2023/740 as

Commission Implementing Decision (EU) 2026/2067 of 11 September 2026 approving derogations from Regulation (EU) 2026/467

Commission Implementing Decision (EU) 2026/2067 of 11 September 2026 approves derogations from Regulation (EU) 2026/467 regarding eligibility conditions of defence products for financial assistance to Ukraine.

Commission Implementing Decision (EU) 2026/2071 of 11 September 2026 approving derogations from Regulation (EU) 2026/467

Commission Implementing Decision (EU) 2026/2071 of 11 September 2026 approves derogations from Regulation (EU) 2026/467 concerning the eligibility conditions of defence products for financial assistance to Ukraine.

Commission Implementing Decision (EU) 2026/2073 of 11 September 2026 approving derogations from Regulation (EU) 2026/467

Commission Implementing Decision (EU) 2026/2073 of 11 September 2026 approves derogations from Regulation (EU) 2026/467 regarding eligibility conditions of defence products for financial assistance to Ukraine.

Commission Implementing Decision (EU) 2026/2081 of 11 September 2026 approving derogations from Regulation (EU) 2026/467

Commission Implementing Decision (EU) 2026/2081 of 11 September 2026 approves derogations from Regulation (EU) 2026/467 regarding eligibility conditions of defence products for financial assistance to Ukraine.

Commission Implementing Decision (EU) 2026/2082 of 11 September 2026 approving derogations from Regulation (EU) 2026/467

Commission Implementing Decision (EU) 2026/2082 of 11 September 2026 approves derogations from Regulation (EU) 2026/467 regarding eligibility conditions of defence products for financial assistance to Ukraine.

Commission Implementing Regulation (EU) 2026/2042 of 11 September 2026 granting a Union authorisation for the biocidal

Commission Implementing Regulation (EU) 2026/2042 of 11 September 2026 grants a Union authorisation for the biocidal product OXTERIL® 350 VHP under Regulation (EU) No 528/2012.

Commission Implementing Regulation (EU) 2026/2044 of 11 September 2026 amending Implementing Regulation (EU) 2024/1767

Commission Implementing Regulation (EU) 2026/2044 amends Implementing Regulation (EU) 2024/1767 to make administrative changes to the Union authorisation of the biocidal product family Sure Lactic Family, effective from 11 September 2026.

Commission Implementing Regulation (EU) 2026/2050 of 11 September 2026 granting a Union authorisation for the biocidal

Commission Implementing Regulation (EU) 2026/2050 of 11 September 2026 grants a Union authorisation for the biocidal product family Hydrogen peroxide biocidal product family under Regulation (EU) No 528/2012.

Commission Implementing Regulation (EU) 2026/2051 of 11 September 2026 granting a Union authorisation for the biocidal

Commission Implementing Regulation (EU) 2026/2051 grants a Union authorisation for the biocidal product family Hydrogen peroxide product family P & G under Regulation (EU) No 528/2012, effective 11 September 2026.

Commission Implementing Regulation (EU) 2026/2054 of 11 September 2026 granting a Union authorisation for the biocidal

Commission Implementing Regulation (EU) 2026/2054 of 11 September 2026 grants a Union authorisation for the biocidal product family Hydrogen peroxides biocides family under Regulation (EU) No 528/2012.

Amending Over-the-Counter Monograph M020: Sunscreen Drug Products for Over-the-Counter Human Use, and Related

FDA has issued a final order amending OTC Monograph M020 for sunscreen drug products, addressing aminobenzoic acid (PABA) and trolamine salicylate ingredients.

Medical Devices; Cardiovascular Devices; Classification of the Cardiovascular Machine Learning-Based Notification

FDA is classifying cardiovascular machine learning-based notification software devices into class II, subject to identified special controls.

Amendment to the International Traffic in Arms Regulations: Prohibited Exports, Imports, and Sales to or From Certain

State Department amends the International Traffic in Arms Regulations to update defense trade restrictions on exports, imports and sales to or from Cyprus.

Eliminating the Discretionary 60-Day Grace Period

DHS proposes removing 8 CFR 214.1(l)(2) to eliminate the discretionary up to 60-day grace period after employment ends for certain nonimmigrant aliens and their dependents before their authorized stay expires.

WCO Secretary General Visits Uzbekistan, Commends Customs Modernization Efforts and Opens Global Canine Forum

The WCO Secretary General visited Uzbekistan to commend its customs modernization efforts and to open the Global Canine Forum.

Document Image System (DIS) Validation of Internal Transaction Number (ITN) for Electronic Export Information (EEI)

CBP has deployed ACE DIS validation of the ITN for EEI submissions (CBP-255) to the Certification Environment, with Production deployment set for October 8, 2026.

Certain Cased Pencils From the People's Republic of China: Preliminary Results of Antidumping Duty Administrative

Commerce issued preliminary results finding dumping of certain cased pencils from China during the December 1, 2024 to November 30, 2025 review period, and invites comments.

Commission Decision (EU) 2026/2030 of 10 September 2026 on signing the agreements amending the Monetary Agreement

Commission Decision (EU) 2026/2030 of 10 September 2026 authorises signing agreements amending the Monetary Agreements between the EU and Andorra and between the EU and San Marino.

Commission Implementing Regulation (EU) 2026/2022 of 10 September 2026 making imports of welded steel mesh originating

Commission Implementing Regulation (EU) 2026/2022 of 10 September 2026 requires registration of imports of welded steel mesh from China and Türkiye, to allow possible retroactive anti-dumping duties.

Commission Implementing Regulation (EU) 2026/2023 of 10 September 2026 making imports of bolted and boltless steel

Commission Implementing Regulation (EU) 2026/2023 of 10 September 2026 requires registration of imports of bolted and boltless steel shelves from China to allow possible retroactive anti-dumping duties.

Commission Implementing Regulation (EU) 2026/2024 of 10 September 2026 amending Implementing Regulation (EU) 2024/2750

Commission Implementing Regulation (EU) 2026/2024 of 10 September 2026 amends Implementing Regulation (EU) 2024/2750 with administrative and minor changes to the Union authorisation of the LANXESS CMIT/MIT biocidal product family.

Commission Implementing Regulation (EU) 2026/2026 of 10 September 2026 amending Implementing Regulation (EU) 2025/524 as

Commission Implementing Regulation (EU) 2026/2028 of 10 September 2026 granting a Union authorisation for the single

Commission Implementing Regulation (EU) 2026/2028 of 10 September 2026 grants a Union authorisation for the single biocidal product ELOCLEAR under Regulation (EU) No 528/2012.

Commission Implementing Regulation (EU) 2026/2053 of 10 September 2026 granting a Union authorisation for the biocidal

Commission Implementing Regulation (EU) 2026/2053 of 10 September 2026 grants a Union authorisation for the biocidal product family Glutaraldehyde formulations under Regulation (EU) No 528/2012.

Political and Security Committee Decision (CFSP) 2026/2062 of 10 September 2026 on the appointment of the EU Mission

Political and Security Committee Decision (CFSP) 2026/2062 of 10 September 2026 appoints a new EU Mission Force Commander for EUMAM Mozambique, repealing Decision (CFSP) 2025/1880.

Political and Security Committee Decision (CFSP) 2026/2063 of 10 September 2026 on the appointment of the EU Mission

Decision (CFSP) 2026/2063 of 10 September 2026 appoints a new EU Mission Force Commander for the EUTM RCA military training mission, repealing Decision (CFSP) 2025/2010.

Fee Rate for Using a Priority Review Voucher in Fiscal Year 2027

FDA announces the FY2027 fee rate for using a priority review voucher on applications for human drug or biological products involving tropical disease, rare pediatric disease, or MCM vouchers.

Green Innovation GmbH; Withdrawal of Food Additive Petition (Animal Use)

FDA is withdrawing, without prejudice to future filing, Food Additive Petition FAP 2323 from Green Innovation GmbH seeking approval of hydrolyzed lignin as a fiber source in animal feed.

Medical Devices; Cardiovascular Devices; Classification of the Extravascular Support for an Arteriovenous Fistula for

FDA is classifying the extravascular support for an arteriovenous fistula for vascular access as a class II medical device subject to identified special controls.

Medical Devices; Cardiovascular Devices; Classification of the Mechanical Deviation Device for Esophageal Protection

FDA is classifying the mechanical deviation device for esophageal protection during cardiac ablation procedures into class II, subject to identified special controls.

Medical Devices; Cardiovascular Devices; Classification of the Temperature Regulation Device for Esophageal Protection

FDA classifies the temperature regulation device for esophageal protection during cardiac ablation procedures into class II, subject to special controls identified in this order.

Medical Devices; Clinical Chemistry and Clinical Toxicology Devices; Classification of the Anti-Tumor Necrosis Factor

FDA classifies the anti-tumor necrosis factor alpha monoclonal antibody test system for inflammatory bowel disease as a class II medical device subject to special controls.

Medical Devices; Ear, Nose, and Throat Devices; Classification of the Cooperative Powered Surgical Assist Device for ENT

FDA is classifying the cooperative powered surgical assist device for ENT surgery into class II with special controls, which will become part of the codified classification language.

Medical Devices; Gastroenterology-Urology Devices; Classification of the Implanted Tibial Electrical Urinary Continence

FDA is classifying the implanted tibial electrical urinary continence device into class II, subject to identified special controls.

Medical Devices; General Hospital and Personal Use Devices; Classification of the Whole Room Microbial Reduction Device

FDA classifies the whole room microbial reduction device into class II, subject to special controls outlined in this order.

Medical Devices; Radiology Devices; Classification of the Vaginal Hydrogel Packing System

FDA is classifying the vaginal hydrogel packing system as a class II medical device subject to special controls, as set out in this order.

Iran-related and Counter Terrorism Designations; Licensing Policy Update under Operation Economic Outcast; Settlement

OFAC updated its sanctions lists with new Iran-related and counter terrorism designations, revised licensing policy under Operation Economic Outcast, and reached a settlement agreement with an individual.

WCO helps Nigeria Customs turn integrity risks into preventive action

WCO is assisting Nigeria Customs in using integrity risk assessment to develop preventive measures against corruption.

ACE Production Standard Invasive Maintenance from 10:00 p.m. ET Saturday, September 12, 2026, to 4:00 a.m. ET Sunday

CSMS #69813698 announces standard invasive maintenance on the ACE production system from 10:00 p.m. ET Saturday, September 12, 2026, to 4:00 a.m. ET Sunday, September 13, 2026.

CBP No. Page Automated Commercial Environment (ACE) Electronic Export Manifest for Rail Cargo

CBP's final rule amends 19 CFR Parts 103, 113, 123, and 192 to require electronic export manifest data in ACE for rail cargo departing the US, effective October 26, 2026, with enforcement from October 26, 2027.

Establishment of Four Customs-Enforcement Areas

AGENCY: U.S. Customs and Border Protection; DHS. ACTION: Establishment of Customs-Enforcement Areas.

Proposed Revocation of One Ruling Letter and Proposed Revocation of Treatment Relating to the Country of Origin of

CBP proposes to revoke one ruling letter and related treatment on the country of origin of outdoor split air conditioning units, inviting comments by October 9, 2026.

Revocation of One Ruling Letter and Revocation of Treatment Relating to the Tariff Classification of a Home Aromatherapy

CBP is revoking one ruling letter and related treatment on the tariff classification of a home aromatherapy plush item under HTSUS, effective for entries on or after November 8, 2026.

Revocation of One Ruling Letter and Revocation of Treatment Relating to the Tariff Classification of a Square Metal

CBP is revoking a ruling letter and related treatment on the tariff classification of a square metal tubing frame for a mechanic's creeper under HTSUS, effective for entries on or after November 8, 2026.

Withdrawal of International Airport Designation of Chalk Seaplane Base . 143 Modification of Seven Ruling Letters and

CBP is modifying seven ruling letters and revoking related treatment on documentary requirements under HTSUS subheading 9801.00.20, effective for entries on or after November 8, 2026.

Preliminary resolution of the administrative antidumping investigation procedure on imports of colored float glass

Preliminary ruling issued in the antidumping investigation on imports of colored float glass from China, regardless of country of origin.

Determination of Regulatory Review Period for Purposes of Patent Extension; ANDEMBRY

FDA has determined the regulatory review period for ANDEMBRY following a patent extension application to the USPTO, as required by law.

Determination of Regulatory Review Period for Purposes of Patent Extension; ANKTIVA

FDA has determined the regulatory review period for the biological product ANKTIVA, supporting a patent extension application filed with the USPTO.

Determination of Regulatory Review Period for Purposes of Patent Extension; ANZUPGO

FDA has determined the regulatory review period for the human drug ANZUPGO, following a patent extension application filed with the USPTO.

Temporary Policies for Compounding Certain Starter Parenteral Nutrition Drug Products for Neonates; Guidance for

FDA issued guidance setting temporary enforcement and regulatory priorities for compounding certain starter parenteral nutrition drug products for neonates by outsourcing facilities, State-licensed pharmacies and Federal facilities.

Vaccines and Related Biological Products Advisory Committee; Notice of Meeting; Establishment of a Public Docket

FDA announces a public meeting and comment docket for the Vaccines and Related Biological Products Advisory Committee on 2027 Southern Hemisphere influenza vaccines.

Transnational Criminal Organizations Designations; Counter Terrorism Designation; Issuance of New and Amended Frequently

OFAC issued new and amended FAQs covering its Transnational Criminal Organizations designations and a Counter Terrorism designation.

Reminder: Only a Few Days Left to Share Your Feedback on ACE

CBP reminds ACE trade community users that the voluntary, anonymous 2026 ACE User Satisfaction Survey remains open until 11:59 p.m. ET on September 11, 2026.

Final resolution of the administrative review procedure of the countervailing duty imposed on imports of children's

Mexico issues final resolution reviewing the countervailing duty on imports of children's bicycles originating in China, regardless of country of origin.

Commission Implementing Decision (EU) 2026/1977 of 8 September 2026 laying down the final import response on behalf of

f the European Parliament and of the Council

Commission Implementing Regulation (EU) 2026/1974 of 8 September 2026 granting a Union authorisation for the single

Commission Implementing Regulation (EU) 2026/1974 of 8 September 2026 grants a Union authorisation for the single biocidal product ERO MN under Regulation (EU) No 528/2012.

Commission Implementing Regulation (EU) 2026/2116 of 8 September 2026 granting a Union authorisation for the biocidal

Commission Implementing Regulation (EU) 2026/2116 of 8 September 2026 grants a Union authorisation for the biocidal product family Christeyns Peracetic Acid Biocidal Product Family under Regulation (EU) No 528/2012.

Corrigendum to Commission Implementing Decision (EU) 2026/1717 of 20 July 2026 on the harmonised standards for gas water

A corrigendum corrects Commission Implementing Decision (EU) 2026/1717 of 20 July 2026 on harmonised standards for gas water heaters supporting Regulation (EU) No 814/2013 and Delegated Regulation (EU) No 812/2013.

Corrigendum to Commission Regulation (EU) 2025/1988 of 2 October 2025 amending Annex XVII to Regulation (EC) No

This corrigendum corrects Commission Regulation (EU) 2025/1988, which amended Annex XVII to Regulation (EC) No 1907/2006 on per- and polyfluoroalkyl substances in firefighting foams.

Iran-related Designations; Counter Terrorism Designations; Updates to Iran-related General Licenses; Issuance of Counter

OFAC adds new Iran-related and counter terrorism designations, updates Iran-related general licenses, and issues a new counter terrorism general license, per accompanying FAQs.

Customs Notice 26-23: United States Surtax Order ( 2026 )

CBSA Customs Notice 26-23 explains that, from September 8, 2026, the United States Surtax Order (2026) applies a 15%, 25% or 50% surtax on value for duty for listed US-origin goods, with specified exemptions.

United States Surtax Order (Steel and Aluminum 2025)

Ottawa, March 12, 2025 Updated: March 27, 2025 Updated: April 8, 2025 Updated: September 1, 2025 Updated: September 7, 2026 1.

Preliminary resolution of the administrative antidumping investigation proceeding on imports of textile-reinforced

Mexico issues a preliminary antidumping ruling on imports of PVC tarpaulins with textile reinforcement originating in China, regardless of country of shipment.

Corrigendum to Commission Implementing Decision (EU) 2025/2499 of 9 December 2025 amending Implementing Decision (EU)

Operation COLIBRI ZAFIRO: Customs and partner agencies join forces to crack down on General Aviation Crime

Operation COLIBRI ZAFIRO reports a joint crackdown by Customs and partner agencies targeting crime linked to General Aviation.