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FDA’s proposed foreign-factory rule would turn vape product listings into SKU-level records. Here is what manufacturers, brands and importers should watch.
FDA Wants Foreign Vape Factories to Register. The Harder Part Is the Product Listing. Read More »
Hawaii’s Act 190 directory requires an FDA marketing-granted order, with first certifications due October 1. What manufacturers, distributors and retailers need to know.
FDA authorized one JUUL2 device and two 18 mg/mL pods—not a product category. The order ties exact configurations to batch testing, marketing controls and postmarket reporting.
FDA Authorized JUUL2: What the Order Covers—and What It Does Not Read More »
Virginia’s October 1 vape rules put retail permits and the OAG product directory on separate tracks. This source-led guide explains fees, penalties, delisting, hardware scope and the unresolved litigation.
Virginia Vape Rules October 1, 2026: Retail Permit vs. Product Directory Read More »
B.C.’s Dec. 15 vape EPR plan date applies to existing producers. See how the rule tests manufacturers, brand owners and importers.
B.C.’s Dec. 15 Vape Recycling Plan Date Turns on Who Counts as the Producer Read More »
Michigan revoked one processor license, recorded another as closed and imposed a $2 million fine. Here is what cannabis vape brands should verify before third-party production.
After Michigan’s $2 Million Processor Order, Brands Should Check Who Holds the License Read More »
California recalled multiple Mwah integrated vaporizers over packaging and labeling attractive to children. Here is the SKU-level approval trail brands should close before production.
California’s Mwah Vape Recall Shows Why Packaging Approval Must Cover Every SKU Read More »
H.R. 6500 created two federal hemp compliance dates: one narrow exclusion begins November 12, while most Section 781 changes move to December 11, 2026.
November 12 vs. December 11, 2026: What the Federal Hemp Deadline Split Actually Says Read More »
