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

Vicks ZzzQuil Liquid Melatonin Syrup Adult 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 ZzzQuil Liquid Melatonin Syrup Adult 8oz plastic bottle sold as single and twin pack

Quantity: 90,522 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: 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

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-1537-2022 · 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