Vicks Children's Botanicals Liquid Daytime
Reason Acidified/Low Acid dietary supplement with no approved process.
Recalled by The Procter & Gamble Company · Cincinnati, OH, United States
Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.
Acidified/Low Acid dietary supplement with no approved process.
These are failures of the safety steps that keep food safe - cooking, pasteurising, keeping cold, sealing - even when no contaminant has yet been found. All processing & sanitation problems recalls.
Vicks Children's Botanicals Liquid Daytime/Nighttime Combo Pack 4oz plastic bottles
Quantity: 82,433 cases
A recall covers only these codes. Compare them with the lot number, best-by date or UPC printed on your package.
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
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FDA's distribution note: 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.
Check the codes, then return or discard. Class II means eating it may cause temporary or reversible health problems. If your package matches the recalled codes, do not eat it - return it to the store or throw it away. FDA lists this recall as terminated: the company has finished removing the product, so it should no longer be on shelves - but it can still be in a freezer or pantry.
FDA files each product of one recall action separately; these share the same FDA event.
Reason Acidified/Low Acid dietary supplement with no approved process.
Reason Acidified/Low Acid dietary supplement with no approved process.
Reason Acidified/Low Acid dietary supplement with no approved process.
Reason Acidified/Low Acid dietary supplement with no approved process.
Reason Illegible Label
Reason Product failed micro testing. Firm sent product for destruction, but was redirected for sale through online store.