[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"fda-warning-letter-liquid-labs-usa-llc-dba-likido-labs-usa-582106-02102021":3,"fda-latest-sync-dates":30},{"id":4,"letter_id":5,"action_type":6,"firm_name":7,"fei_number":8,"issuing_office":9,"subject":10,"posted_date":11,"action_taken_date":12,"response_letter_date":8,"closeout_date":8,"case_status":13,"letter_url":14,"reference_number":15,"marcs_cms_no":16,"product_type":17,"delivery_method":18,"recipient_name":19,"recipient_title":8,"body_html":20,"body_text":21,"body_fetched_at":22,"medical_device_id":8,"raw":23,"created_at":28,"updated_at":29},3535,"liquid-labs-usa-llc-dba-likido-labs-usa-582106-02102021","Warning Letter","Liquid Labs USA, LLC d\u002Fb\u002Fa Likido Labs USA",null,"Center for Tobacco Products","Family Smoking Prevention and Tobacco Control Act\u002FAdulterated\u002FMisbranded","2021-02-16","2021-02-10","Issued","https:\u002F\u002Fwww.fda.gov\u002Finspections-compliance-enforcement-and-criminal-investigations\u002Fwarning-letters\u002Fliquid-labs-usa-llc-dba-likido-labs-usa-582106-02102021","ER1900023","582106","Tobacco","VIA UPS and Electronic Mail","Justin A. Jason","\n\n                            \n                            \n                            \n                            \n                                              \n  \n \n\n                 \n\n  \u003Chr>\n \n\n\u003Cdiv class=\"inset-column\">\n  \u003Cdl class=\"lcds-description-list--grid\">\n\n              \u003Cdt class=\"cell-1_1\">Delivery Method:\u003C\u002Fdt> \n        \u003Cdd class=\"cell-2_1\">VIA UPS and Electronic Mail\n                                                                                                                                                                                                                                                                                                                                                                                                                              \u003C\u002Fdd>\n      \n              \u003Cdt class=\"cell-1_2\">Reference #:\u003C\u002Fdt> \n        \u003Cdd class=\"cell-2_2\">ER1900023\u003C\u002Fdd>\n      \n              \u003Cdt class=\"cell-1_3\">Product:\u003C\u002Fdt> \n        \u003Cdd class=\"cell-2_3\">Tobacco                          \n            \n            \n            \n            \n            \n            \n            \n             \n            \n            \n            \n              \n            \n            \n            \u003C\u002Fdd>\n      \n          \u003C\u002Fdl>\n  \u003C\u002Fdiv>            \n\n\n\u003Chr>\n\n\u003Cdiv class=\"row inset-column\">\n  \u003Cdiv class=\"col-xs-12 col-md-6\">\n    \u003Cdl class=\"\">\n\n        \u003Cdt>Recipient:\u003C\u002Fdt>\n\n                      \u003Cdd>\n  \u003Cdiv class=\"field field--name-field-recipient-name field--type-string field--label-above\">\n    \u003Cdiv class=\"field--label\">Recipient Name\u003C\u002Fdiv>\n              \u003Cdiv class=\"field--item\">Justin A. Jason\u003C\u002Fdiv>\n          \u003C\u002Fdiv>\n\u003C\u002Fdd>\n                                \u003Cdd>\n  \u003Cdiv class=\"field field--name-field-recipient-title field--type-string field--label-above\">\n    \u003Cdiv class=\"field--label\">Recipient Title\u003C\u002Fdiv>\n              \u003Cdiv class=\"field--item\">Managing Member\u003C\u002Fdiv>\n          \u003C\u002Fdiv>\n\u003C\u002Fdd>\n          \n            \u003Cdd>Liquid Labs USA, LLC d\u002Fb\u002Fa Likido Labs USA\u003C\u002Fdd>\n\n          \n                      \u003Cdd>\u003Cp class=\"address\" translate=\"no\">\u003Cspan class=\"address-line1\">2663 Saturn Street\u003C\u002Fspan>\u003Cbr>\n\u003Cspan class=\"locality\">Brea\u003C\u002Fspan>, \u003Cspan class=\"administrative-area\">CA\u003C\u002Fspan> \u003Cspan class=\"postal-code\">92821-6785\u003C\u002Fspan>\u003Cbr>\n\u003Cspan class=\"country\">United States\u003C\u002Fspan>\u003C\u002Fp>\u003C\u002Fdd>\n          \n          \n            \n            \u003Cdd>\u003C!-- Loop this field. For FDA Office content type. Display the Other contact channel is a dd span with an icon-->\n\n    \u003C\u002Fdd>\u003Cdd>\u003Cspan class=\"fa fa-envelope\" aria-hidden=\"true\">\u003C\u002Fspan>\u003Ca href=\"mailto:justin@likidolabs.com\"> justin@likidolabs.com\u003C\u002Fa>\u003C\u002Fdd>\n\n          \n    \u003C\u002Fdl>\n  \u003C\u002Fdiv>            \n\n       \u003Cdiv class=\"col-xs-12 col-md-6\">\n    \u003Cdl class=\"\">\n          \n          \u003Cdt>Issuing Office:\u003C\u002Fdt>\n        \n         \n          \u003Cdd>Center for Tobacco Products\u003C\u002Fdd>\n        \n         \n          \u003Cdd>\u003Cp class=\"address\" translate=\"no\">\u003Cspan class=\"country\">United States\u003C\u002Fspan>\u003C\u002Fp>\u003C\u002Fdd>\n        \n        \n        \n        \n        \n    \u003C\u002Fdl>\n    \u003Cdl class=\"\"> \n      \n    \u003C\u002Fdl>\n  \u003C\u002Fdiv>  \n      \n\u003C\u002Fdiv>\n\n \n\n \n\n\u003Chr>\n\n\u003Cp class=\"text-align-center\">\u003Cstrong>WARNING LETTER\u003C\u002Fstrong>\u003C\u002Fp>\u003Cp class=\"text-align-center\">\u003Cstrong>Feb 10, 2021\u003C\u002Fstrong>\u003C\u002Fp>\u003Cp>Dear Mr. Jason:\u003C\u002Fp>\u003Cp>The Center for Tobacco Products of the U.S. Food and Drug Administration (FDA) has reviewed your submissions to the FDA and our inspection records, and determined that Liquid Labs USA, LLC, d\u002Fb\u002Fa Likido Labs USA manufactures and distributes e-liquid products for commercial distribution in the United States, and that the e-liquid products are manufactured and offered for sale or distribution to customers in the United States. Under section 201 (rr) of the Federal Food, Drug, and Cosmetic Act (FD&C Act) (21 U.S.C. § 321(rr)), as amended by the Family Smoking Prevention and Tobacco Control Act, these products are tobacco products because they are made or derived from tobacco and intended for human consumption. Certain tobacco products, including e-liquids, are subject to FDA's jurisdiction under section 901 (b) of the FD&C Act (21 U.S.C. § 387a(b)).\u003C\u002Fp>\u003Cp>FDA has determined that your Vape SZNS Salty SZN Porn Berry Salts, Vape SZNS Salty SZN Kapital Grape Salts, and Vape SZNS Salty SZN Neon Sours Salts e-liquids are adulterated under section 902(6)(A) of the FD&C Act (21 U.S.C. § 387b(6)(A)) for not having a required FDA marketing authorization order in effect and\u002For misbranded under section 903(a)(6) of the FD&C Act (21 U.S.C. § 387c(a)(6)) because a required notice or other information respecting the products was not provided.\u003C\u002Fp>\u003Cp>\u003Cstrong>New Tobacco Products Without Required Marketing Authorization Are Adulterated and\u002For Misbranded\u003C\u002Fstrong>\u003C\u002Fp>\u003Cp>FDA has determined that you manufacture, sell, and\u002For distribute to customers in the United States the following a-liquid products without a marketing authorization order: Vape SZNS Salty SZN Porn Berry Salts, Vape SZNS Salty SZN Kapital Grape Salts, and Vape SZNS Salty SZN Neon Sours Salts.\u003C\u002Fp>\u003Cp>The FD&C Act generally requires premarket review for any \"new tobacco product,\" which means any tobacco product that was not commercially marketed in the United States as of February 15, 2007, or any modification of a tobacco product where the modified product was commercially marketed in the United States after February 15, 2007 (section 91 0(a) of the FD&C Act; 21 U.S.C. § 387j(a)). A marketing authorization order under section 910(c)(1)(A)(i) of the FD&C Act (21 U.S.C. § 387j(c)(1)(A)(i)) is required for a new tobacco product unless (1) FDA issues an order finding the product substantially equivalent to a predicate tobacco product (section 910(a)(2)(A) of the FD&C Act) or (2) FDA issues an order finding the product to be exempt from the requirements of substantial equivalence and you make the required submission under section 905U)(1 )(A)(ii) of the FD&C Act (21 U.S.C. § 387e(j)(1)(A)(ii)). All deemed products that meet the definition of a \"new tobacco product,\" including e-liquids, are subject to the premarket requirements in sections 910 and 905 of the FD&C Act.\u003C\u002Fp>\u003Cp>FDA has determined that the following e-liquids products were not commercially marketed in the United States as of February 15, 2007: Vape SZNS Salty SZN Porn Berry Salts, Vape SZNS Salty SZN Kapital Grape Salts, and Vape SZNS Salty Neon Sours.\u003C\u002Fp>\u003Cp>These products are required to have premarket review and do not have FDA marketing authorization orders in effect under section 910(c)(1)(A)(i) of the FD&C Act. Therefore, they are adulterated under section 902(6)(A) of the FD&C Act. In addition, they are misbranded under section 903(a)(6) of the FD&C Act because a notice or other information respecting these products was not provided as required by section 905(j) of the FD&C Act (21 U.S.C. § 387e(j)). The introduction into interstate commerce of any tobacco product that is adulterated or misbranded is a prohibited act under section 301 (a) of the' FD&C Act (21 U.S.C. § 331 (a)). Additionally, to the extent that a report was required under section 905U) of the FD&C Act, the failure to provide such report is a prohibited act under section 301 (p) of the FD&C Act (21 U.S.C. § 331(p)).\u003C\u002Fp>\u003Cp>\u003Cstrong>Conclusion and Requested Actions\u003C\u002Fstrong>\u003C\u002Fp>\u003Cp>The violations discussed in this letter do not necessarily constitute an exhaustive list. You should immediately correct the violations that are referenced above, as well as violations that are the same as or similar to the one stated above, and take any necessary actions to bring your tobacco products into compliance with the FD&C Act.\u003C\u002Fp>\u003Cp>It is your responsibility to ensure that your tobacco products comply with each applicable provision of the FD&C Act and FDA's implementing regulations. Failure to ensure full compliance with the FD&C Act may result in FDA initiating further action without notice, including, but not limited to, civil money penalties, criminal prosecution, seizure, and\u002For injunction. Please note that any adulterated and\u002For misbranded tobacco products offered for import into the United States are subject to detention and refusal of admission.\u003C\u002Fp>\u003Cp>Please submit a written response to this letter within 15 working days from the date of receipt describing your corrective actions, including the dates on which you discontinued the violative sale, and\u002For distribution of these tobacco products and your plan for maintaining compliance with the FD&C Act. If you do not believe that your products are in violation of the FD&C Act, include your reasoning and any supporting information for our consideration. You can find the FD&C Act through links on FDA's homepage at http:\u002F\u002Fwww.fda.gov.\u003C\u002Fp>\u003Cp>Please note your reference number, ER1900023, in your response and direct your response to the following address:\u003C\u002Fp>\u003Cp>DEM-WL Response, Office of Compliance and Enforcement\u003Cbr>FDA Center for Tobacco Products\u003Cbr>c\u002Fo Document Control Center\u003Cbr>Building 71, Room G335\u003Cbr>10903 New Hampshire Avenue\u003Cbr>Silver Spring, MD 20993-0002\u003C\u002Fp>\u003Cp>If you have any questions about the content of this letter, please contact Lillian Ortega at (240) 402-9041 or Lillian.Ortega@fda.hhs.gov.\u003C\u002Fp>\u003Cp>Sincerely,\u003Cbr>\u002FS\u002F\u003C\u002Fp>\u003Cp>Ann Simoneau, J.D.\u003Cbr>Director\u003Cbr>Office of Compliance and Enforcement\u003Cbr>Center for Tobacco Products\u003C\u002Fp>\n\n\u003C!--BEGIN QUALTRICS WEBSITE FEEDBACK SNIPPET-->\n\u003C!--BEGIN QUALTRICS WEBSITE FEEDBACK SNIPPET-->\n\n\n\n              \n                                            \n              \n            ","Delivery Method:\n\nVIA UPS and Electronic Mail\n\nReference #:\n\nER1900023\n\nProduct:\n\nTobacco\n\nRecipient:\n\nRecipient Name\n\nJustin A. Jason\n\nRecipient Title\n\nManaging Member\n\nLiquid Labs USA, LLC d\u002Fb\u002Fa Likido Labs USA\n\n2663 Saturn Street\n\nBrea, CA 92821-6785\n\nUnited States\n\njustin@likidolabs.com\n\nIssuing Office:\n\nCenter for Tobacco Products\n\nUnited States\n\nWARNING LETTER\nFeb 10, 2021\nDear Mr. Jason:\nThe Center for Tobacco Products of the U.S. Food and Drug Administration (FDA) has reviewed your submissions to the FDA and our inspection records, and determined that Liquid Labs USA, LLC, d\u002Fb\u002Fa Likido Labs USA manufactures and distributes e-liquid products for commercial distribution in the United States, and that the e-liquid products are manufactured and offered for sale or distribution to customers in the United States. Under section 201 (rr) of the Federal Food, Drug, and Cosmetic Act (FD&C Act) (21 U.S.C. § 321(rr)), as amended by the Family Smoking Prevention and Tobacco Control Act, these products are tobacco products because they are made or derived from tobacco and intended for human consumption. Certain tobacco products, including e-liquids, are subject to FDA's jurisdiction under section 901 (b) of the FD&C Act (21 U.S.C. § 387a(b)).\nFDA has determined that your Vape SZNS Salty SZN Porn Berry Salts, Vape SZNS Salty SZN Kapital Grape Salts, and Vape SZNS Salty SZN Neon Sours Salts e-liquids are adulterated under section 902(6)(A) of the FD&C Act (21 U.S.C. § 387b(6)(A)) for not having a required FDA marketing authorization order in effect and\u002For misbranded under section 903(a)(6) of the FD&C Act (21 U.S.C. § 387c(a)(6)) because a required notice or other information respecting the products was not provided.\nNew Tobacco Products Without Required Marketing Authorization Are Adulterated and\u002For Misbranded\nFDA has determined that you manufacture, sell, and\u002For distribute to customers in the United States the following a-liquid products without a marketing authorization order: Vape SZNS Salty SZN Porn Berry Salts, Vape SZNS Salty SZN Kapital Grape Salts, and Vape SZNS Salty SZN Neon Sours Salts.\nThe FD&C Act generally requires premarket review for any \"new tobacco product,\" which means any tobacco product that was not commercially marketed in the United States as of February 15, 2007, or any modification of a tobacco product where the modified product was commercially marketed in the United States after February 15, 2007 (section 91 0(a) of the FD&C Act; 21 U.S.C. § 387j(a)). A marketing authorization order under section 910(c)(1)(A)(i) of the FD&C Act (21 U.S.C. § 387j(c)(1)(A)(i)) is required for a new tobacco product unless (1) FDA issues an order finding the product substantially equivalent to a predicate tobacco product (section 910(a)(2)(A) of the FD&C Act) or (2) FDA issues an order finding the product to be exempt from the requirements of substantial equivalence and you make the required submission under section 905U)(1 )(A)(ii) of the FD&C Act (21 U.S.C. § 387e(j)(1)(A)(ii)). All deemed products that meet the definition of a \"new tobacco product,\" including e-liquids, are subject to the premarket requirements in sections 910 and 905 of the FD&C Act.\nFDA has determined that the following e-liquids products were not commercially marketed in the United States as of February 15, 2007: Vape SZNS Salty SZN Porn Berry Salts, Vape SZNS Salty SZN Kapital Grape Salts, and Vape SZNS Salty Neon Sours.\nThese products are required to have premarket review and do not have FDA marketing authorization orders in effect under section 910(c)(1)(A)(i) of the FD&C Act. Therefore, they are adulterated under section 902(6)(A) of the FD&C Act. In addition, they are misbranded under section 903(a)(6) of the FD&C Act because a notice or other information respecting these products was not provided as required by section 905(j) of the FD&C Act (21 U.S.C. § 387e(j)). The introduction into interstate commerce of any tobacco product that is adulterated or misbranded is a prohibited act under section 301 (a) of the' FD&C Act (21 U.S.C. § 331 (a)). Additionally, to the extent that a report was required under section 905U) of the FD&C Act, the failure to provide such report is a prohibited act under section 301 (p) of the FD&C Act (21 U.S.C. § 331(p)).\nConclusion and Requested Actions\nThe violations discussed in this letter do not necessarily constitute an exhaustive list. You should immediately correct the violations that are referenced above, as well as violations that are the same as or similar to the one stated above, and take any necessary actions to bring your tobacco products into compliance with the FD&C Act.\nIt is your responsibility to ensure that your tobacco products comply with each applicable provision of the FD&C Act and FDA's implementing regulations. Failure to ensure full compliance with the FD&C Act may result in FDA initiating further action without notice, including, but not limited to, civil money penalties, criminal prosecution, seizure, and\u002For injunction. Please note that any adulterated and\u002For misbranded tobacco products offered for import into the United States are subject to detention and refusal of admission.\nPlease submit a written response to this letter within 15 working days from the date of receipt describing your corrective actions, including the dates on which you discontinued the violative sale, and\u002For distribution of these tobacco products and your plan for maintaining compliance with the FD&C Act. If you do not believe that your products are in violation of the FD&C Act, include your reasoning and any supporting information for our consideration. You can find the FD&C Act through links on FDA's homepage at http:\u002F\u002Fwww.fda.gov.\nPlease note your reference number, ER1900023, in your response and direct your response to the following address:\nDEM-WL Response, Office of Compliance and Enforcement\nFDA Center for Tobacco Products\nc\u002Fo Document Control Center\nBuilding 71, Room G335\n10903 New Hampshire Avenue\nSilver Spring, MD 20993-0002\nIf you have any questions about the content of this letter, please contact Lillian Ortega at (240) 402-9041 or Lillian.Ortega@fda.hhs.gov.\nSincerely,\n\u002FS\u002F\nAnn Simoneau, J.D.\nDirector\nOffice of Compliance and Enforcement\nCenter for Tobacco Products","2026-08-20T03:22:57.279+00:00",[24,25,26,9,10,27,27,27],"\u003Ctime datetime=\"2021-02-16T05:00:00Z\">02\u002F16\u002F2021\u003C\u002Ftime>\n","\u003Ctime datetime=\"2021-02-10T05:00:00Z\">02\u002F10\u002F2021\u003C\u002Ftime>\n","\u003Ca href=\"\u002Finspections-compliance-enforcement-and-criminal-investigations\u002Fwarning-letters\u002Fliquid-labs-usa-llc-dba-likido-labs-usa-582106-02102021\">Liquid Labs USA, LLC d\u002Fb\u002Fa Likido Labs USA\u003C\u002Fa>","","2026-08-18T06:42:29.460824+00:00","2026-08-20T03:22:59.41592+00:00",{"510k":31,"classification":32,"enforcement":33,"event":34,"pma":35,"warning_letter":36},"2026-08-18T06:35:18.347+00:00","2026-08-18T05:52:53.75+00:00","2026-08-18T08:01:54.918+00:00","2026-08-19T02:58:35.995+00:00","2026-08-18T06:36:30.549+00:00","2026-08-20T03:28:02.95+00:00"]