FDA recall record
Vicks ZzzQuil Liquid Melatonin Syrup Adult 8oz plastic bottle sold as single and twin pack
FDA classification. FDA Class I, II, and III are not the same as USDA FSIS classifications and are not a cross-agency safety score.
FDA listed a termination date of August 15, 2024. openFDA does not treat this as a live recall-status tracker.
Product described in an FDA recall
Vicks ZzzQuil Liquid Melatonin Syrup Adult 8oz plastic bottle sold as single and twin pack
Reason
Acidified/Low Acid dietary supplement with no approved process.
Products involved
Product descriptions are copied from the FDA recall record. They are not a current catalog and are not automatically matched to WhoMadeMyFood product pages.
Vicks ZzzQuil Liquid Melatonin Syrup Adult 8oz plastic bottle sold as single and twin pack
Code information listed by FDA
Batch Numbers: 10324334R1, 10324334R2, 10324334R3, 10324334R4, 10324334R5, 10324334R6,10534334R1, 10534334R2, 10564334R1, 10564334R2, 10764334R1, 11234334R1, 11234334R2, 11244334R1, 12164334N1, 12164334N2, 12864334N1, 20074334N1, 20074334S1, 20134334N1, 20134334N2, 1032C60401, 1032C60402, 1032C60403, 1053C60401, 1053C60402, 1056C60401, 1056C60402, 1076C60401, 1076C60402, 1076C60403, 1116C60410, 1123C60402, 1123C60404, 1124C60401, 1147C60401, 1216C60404, 1217C60401, 1235C60402, 1251C60403, 1251C60404, 1286C60402, 1286C60403, 1286C60404, 1286C60405, 1301C60403, 2007C60402, 2007C60403, 2007C6041, 2013C60401, 2035C60401, 2035C60402, 2080C60401, 2091C60401, 2096C60401 Lot Numbers: 10324334R1, 10324334R2, 10324334R3, 10324334R4, 10324334R5, 10324334R6, 10534334R1, 10534334R2, 10564334R1, 10564334R2, 10764334R1, 11234334R1, 11234334R2, 11244334R1, 12164334N1, 12164334N2, 12864334N1, 20074334N1, 20074334S1, 20134334N1,, 20134334N2, 1032C60401, 1032C60402, 1032C60403, 1053C60401, 1053C60402, 1056C60401, 1056C60402, 1076C60401, 1076C60402, 1076C60403, 1116C60410, 1123C60402, 1123C60404, 1124C60401, 1147C60401, 1216C60404, 1217C60401, 1235C60402, 1251C60403, 1251C60404, 1286C60402, 1286C60403, 1286C60404, 1286C60405, 1301C60403, 2007C60402, 2007C60403, 2007C6041, 2013C60401, 2035C60401, 2035C60402, 2080C60401, 2091C60401, 2096C60401 Product Number: 80358162,80349921 Item UPC: 80358162,323900040151 Case UPC: 10323900043074,10323900040158 Expiration Dates: 10324334R1 07/31/2022, 10324334R2 07/31/2022, 10324334R3 07/31/2022, 10324334R4 07/31/2022, 10324334R5 07/31/2022, 10324334R6 07/31/2022, 10534334R1 07/31/2022, 10534334R2 07/31/2022, 10564334R1 07/31/2022, 10564334R2 07/31/2022, 10764334R1 08/31/2022, 11234334R1 -10/31/2022 , 11234334R2 10/31/2022, 11244334R1 10/31/2022, 12164334N1 01/31/2023, 12164334N2 01/31/2023, 12864334N1 03/31/2023, 20074334N1 06/30/2023, 20074334S1 06/30/2023 , 20134334N1 06/30/2023, 20134334N2 06/30/2023, 1032C60401 07/31/2022, 1032C60402 07/31/2022, 1032C60403 07/31/2022, 1053C60401 07/31/2022, 1053C60402 07/31/2022, 1056C60401 07/31/2022, 1056C60402 07/31/2022, 1076C60401 08/31/2022, 1076C60402 08/31/2022, 1076C60403 08/31/2022, 1116C60410 09/30/2022, 1123C60402 10/31/2022, 1123C60404 10/31/2022, 1124C60401 10/31/2022, 1147C60401 10/31/2022, 1216C60404 01/31/2023, 1217C60401 01/31/2023, 1235C60402 01/31/2023, 1251C60403 02/28/2023, 1251C60404 02/28/2023, 1286C60402 03/31/2023, 1286C60403 03/31/2023, 1286C60404 03/31/2023, 1286C60405 03/31/2023, 1301C60403 03/31/2023, 2007C60402 - , 2007C60403 06/30/2023, 2007C6041 06/30/2023, 2013C60401 06/30/2023, 2035C60401 07/31/2023, 2035C60402 07/31/2023, 2080C60401 08/31/2023, 2091C60401 09/30/2023, 2096C60401 09/30/2023
Distribution and firm information
Recalling firm listed by FDA: The Procter & Gamble Company
Firm location listed by FDA: Cincinnati, OH, United States
Distribution reported by FDA: Alaska, Alabama, Arkansas, Arizona, California, Colorado, Connecticut, Delaware, Florida, Georgia, Hawaii, Iowa, Idaho, Illinois, Indiana, Kansas, Kentucky, Louisiana, Maine, Massachusetts, Maryland, Michigan, Minnesota, Missouri, Mississippi, North Carolina, North Dakota, New Hampshire, New Jersey, Nevada, New York, Ohio, Oklahoma, Oregon, Pennsylvania, Rhode Island, South Carolina, South Dakota, Tennessee, Texas, Utah, Virginia, Washington, Wisconsin, and West Virginia.
Product quantity listed by FDA: 90,522 cases
Source
Source: U.S. Food and Drug Administration (FDA), openFDA food enforcement reports.
Official FDA openFDA food enforcement record
Identifying an FDA recall record does not imply FDA endorsement of WhoMadeMyFood. Methodology.