FDA recall record
Vicks Children's Botanicals Liquid Daytime/Nighttime Combo Pack 4oz plastic bottles
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 Children's Botanicals Liquid Daytime/Nighttime Combo Pack 4oz plastic bottles
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 Children's Botanicals Liquid Daytime/Nighttime Combo Pack 4oz plastic bottles
Code information listed by FDA
Batch Numbers: 0240C60405, 0314C60402, 11664334R1, 11664334R2, 11664334R3, 11664334R4, 11664334R5, 11664334E1, 12164334E1, 12164334E2, 12164334Y1, 12164334Y2, 12164334Y3, 12164334Y4, 12164334Y5, 12164334Y6, 12184334E1, 12184334E2, 12184334E3, 12184334E4, 12184334Y1, 12184334Y2, 12184334Y3, 12184334Y4, 12374334D1, 12374334D2, 12374334E0, 12374334E1, 12374334E2, 12374334E3, 12374334E4, 12374334E5, 12374334E6, 12374334E7, 12374334E8, 12374334E9, 12374334EA, 12374334Y1, 12374334Y2, 13214334D1, 13214334D2, 13214334J1, 13214334K0, 13214334K1, 13214334K2, 13214334K3, 13214334K4, 13214334K5, 13214334K6, 13214334K7, 13214334K8, 13214334K9, 13214334P1, 13214334P2, 13624334S1, 20124334E1, 20124334E2, 20124334E3, 20124334K1, 20124334K2, 20124334K3, 20124334K4, 20384334E1, 20384334E2, 20384334E3 Lot Numbers: 0240C60405, 0314C60402, 11664334R1, 11664334R2, 11664334R3, 11664334R4, 11664334R5, 11664334E1, 12164334E1, 12164334E2, 12164334Y1, 12164334Y2, 12164334Y3, 12164334Y4, 12164334Y5, 12164334Y6, 12184334E1, 12184334E2, 12184334E3, 12184334E4, 12184334Y1, 12184334Y2, 12184334Y3, 12184334Y4, 12374334D1, 12374334D2, 12374334E0, 12374334E1, 12374334E2, 12374334E3, 12374334E4, 12374334E5, 12374334E6, 12374334E7, 12374334E8, 12374334E9, 12374334EA, 12374334Y1, 12374334Y2, 13214334D1, 13214334D2, 13214334J1, 13214334K0, 13214334K1, 13214334K2, 13214334K3, 13214334K4, 13214334K5, 13214334K6, 13214334K7, 13214334K8, 13214334K9, 13214334P1, 13214334P2, 13624334S1, 20124334E1, 20124334E2, 20124334E3, 20124334K1, 20124334K2, 20124334K3, 20124334K4, 20384334E1, 20384334E2, 20384334E3 Product Number: 80338569, 80365757 Item UPC: 323900041073 Case UPC: 10323900041070 Expiration Dates: 0240C60405 07/31/2022, 0314C60402 10/31/2022, 11664334R2 - 05/31/2023, 11664334R3 - 05/31/2023, 11664334R4 - 05/31/2023, 11664334R5 - 05/31/2023, 11664334E1 - 05/31/2023, 12164334E1 07/31/2023, 12164334E2 - 07/31/2023, 12164334Y1 - 07/31/2023, 12164334Y2 - 07/31/2023, 12164334Y3 - 07/31/2023, 12164334Y4 - 07/31/2023, 12164334Y5 - 07/31/2023, 12164334Y6 - 07/31/2023, 12184334E1 - 07/31/2023, 12184334E2 - 07/31/2023, 12184334E3 - 07/31/2023, 12184334E4 - 07/31/2023, 12184334Y1 - 07/31/2023, 12184334Y2 - 07/31/2023, 12184334Y3 - 07/31/2023, 12184334Y4 - 07/31/2023, 12374334D1 - 07/31/2023, 12374334D2 - 07/31/2023, 12374334E0 - 07/31/2023, 12374334E1 - 07/31/2023, 12374334E2 - 07/31/2023, 12374334E3 - 07/31/2023, 12374334E4 - 07/31/2023, 12374334E5 - 07/31/2023, 12374334E6 - 07/31/2023, 12374334E7 - 07/31/2023, 12374334E8 - 07/31/2023, 12374334E9 - 07/31/2023, 12374334EA - 07/31/2023, 12374334Y1 - 07/31/2023, 12374334Y2 - 07/31/2023, 13214334D1 10/31/2023, 13214334D2 - 10/31/2023, 13214334J1 - 10/31/2023, 13214334K0 - 10/31/2023, 13214334K1 - 10/31/2023, 13214334K2 - 10/31/2023, 13214334K3 - 10/31/2023, 13214334K4 - 10/31/2023, 13214334K5 - 10/31/2023, 13214334K6 - 10/31/2023, 13214334K7 - 10/31/2023, 13214334K8 - 10/31/2023, 13214334K9 - 10/31/2023, 13214334P1 - 10/31/2023, 13214334P2 - 10/31/2023, 13624334S1 10/31/2023, 20124334E1 12/31/2023, 20124334E2 - 12/31/2023, 20124334E3 - 12/31/2023, 20124334K1 - 12/31/2023, 20124334K2 - 12/31/2023, 20124334K3 - 12/31/2023, 20124334K4 - 12/31/2023, 20384334E1 01/31/2024, 20384334E2 01/31/2024, 20384334E3 10/31/2024
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: 82,433 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.