Vicks Children's Botanicals Liquid Daytime/Nighttime Combo Pack
Reason Acidified/Low Acid dietary supplement with no approved process.
Vicks Children's Botanicals Liquid Nighttime 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 Nighttime 4oz plastic bottle
Quantity: 18,490 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: 0240C60404, 1166C60401, 1218C60401, 1237C60401, 1321C60401,1321C60402, 1321C604Q1, 2038C60401, 2152C60401 , 2153C60401 Lot Numbers: 0240C60404, 1166C60401, 1218C60401, 1237C60401, 1321C60401, 1321C60402, 1321C604Q1, 2038C60401, 2152C60401, 2153C60401 Product Number: 80338364 Item UPC: 323900041066 Case UPC: 10323900041063 Expiration Dates: 0240C60404 07/31/2022, 1166C60401 05/31/2023, 1218C60401 07/31/2023, 1237C60401 07/31/2023, 1321C60401 10/31/2023, 1321C60402 10/31/2023, 1321C604Q1 10/31/2023, 2038C60401 01/31/2024, 2152C60401 05/31/2024, 2153C60401 05/31/2024
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-1535-2022 · 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.
Vicks Children's Botanicals Liquid Daytime
Reason Acidified/Low Acid dietary supplement with no approved process.
Vicks ZzzQuil Liquid Melatonin Syrup Pediatric
Reason Acidified/Low Acid dietary supplement with no approved process.
Vicks ZzzQuil Liquid Melatonin Syrup Adult
Reason Acidified/Low Acid dietary supplement with no approved process.
Other recalls by The Procter & Gamble Company
Meta Psyllium Fiber Capsules packaged as
Reason Illegible Label
Align Digestive De-Stress Capsules
Reason Product failed micro testing. Firm sent product for destruction, but was redirected for sale through online store.