Food Recall Check
Class II · Moderate risk Terminated Initiated Jul 12, 2022 (4 years ago)

Vicks Children's Botanicals Liquid Daytime recall

Recalled by The Procter & Gamble Company · Cincinnati, OH, United States

Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.

Why it was recalled

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.

What was recalled

Vicks Children's Botanicals Liquid Daytime 4oz plastic bottle

Quantity: 34,526 cases

Lot codes, dates and UPCs

A recall covers only these codes. Compare them with the lot number, best-by date or UPC printed on your package.

Batch Numbers: 0240C60402, 0279C60401, 1176C60401, 1216C60403, 1237C60402, 1321C60404, 2012C60401, 2012C60402, 2012C60403, 2110C60401 Lot Numbers: 0240C60402, 0279C60401, 1176C60401, 1216C60403, 1237C60402, 1321C60404, 2012C60401, 2012C60402, 2012C60403, 2110C60401 Product Number: 80338363 Item UPC: 323900041059 Case UPC: 10323900041056 Expiration Dates: 0240C60402 07/31/2022, 0279C60401 09/30/2022 , 1176C60401 05/31/2023, 1216C60403 07/31/2023, 1237C60402 07/31/2023, 1321C60404 10/31/2023, 2012C60401 12/31/2023, 2012C60402 12/31/2023, 2012C60403 12/31/2023, 2110C60401 03/31/2024

Where it was sold

Alaska Alabama Arkansas Arizona California Colorado Connecticut Delaware Florida Georgia Hawaii Iowa Idaho Illinois Indiana Kansas Kentucky Louisiana Massachusetts Maryland Maine 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 West Virginia

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.

Recalling firm
The Procter & Gamble Company
Initiated by
Voluntary: Firm initiated
Recall initiated
Jul 12, 2022
In FDA report of
Aug 10, 2022
Terminated
Aug 15, 2024
FDA recall number
F-1534-2022 · event 90615
Official record
FDA enforcement report search

Also recalled with it (4 more products)

FDA files each product of one recall action separately; these share the same FDA event.

Other recalls by The Procter & Gamble Company

Class II · Moderate risk Terminated Other

Align Digestive De-Stress Capsules

Reason Product failed micro testing. Firm sent product for destruction, but was redirected for sale through online store.

The Procter & Gamble Company F-1012-2022