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The FDA notes in the update that when it announced the issuance of the MDOs, the agency stated that some of the company’s study findings “raised concerns due to insufficient and conflicting data regarding genotoxicity and potentially harmful chemicals leaching from the company’s proprietary e-liquid pods, which precluded the FDA from completing a full toxicological review of the products.” Additional Review and Legal Developments On July 5, 2022, the FDA administratively stayed the MDOs after determining that certain scientific issues warranted additional review

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This patent enforcement action builds off previous actions Juul Labs pursued at the ITC, targeting a broad range of importers of unauthorized Juul-compatible products, including Eonsmoke and Ziip Labs