CLASS II Food recall · Reported 10 Aug 2022 · FDA Enforcement Report
Vicks ZzzQuil Liquid Melatonin Syrup Adult sold as single recalled
The Procter & Gamble is recalling Vicks ZzzQuil Liquid Melatonin Syrup Adult sold as single and twin pack, distributed in 45 states. The recall was initiated on 12 Jul 2022 and the FDA has classified it as Class II.
Check your package
Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.
Recall details
- Recall number
- F-1537-2022
- FDA event ID
- 90615
- Recalling firm
- The Procter & Gamble, Cincinnati, OH
- Brand
- Vicks ZzzQuil
- Classification
- Class II
- Status
- Terminated
- Recall initiated
- 12 Jul 2022
- FDA classified
- 3 Aug 2022
- Reported
- 10 Aug 2022
- Type
- Voluntary: Firm initiated
- Customers notified by
- Reason category
- Foreign Material
- Product category
- Honey & Syrup
Timeline
| 12 Jul 2022 | Recall initiated by company | |
| 3 Aug 2022 | Classified by FDA | +22 days |
| 10 Aug 2022 | Published in enforcement report | +7 days |
Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.
Reason for recall
Acidified/Low Acid dietary supplement with no approved process.
Foreign material recalls cover pieces of metal, plastic, glass, wood or other objects that got into the product during processing and could cause injury if eaten.
Product as listed by the FDA
Vicks ZzzQuil Liquid Melatonin Syrup Adult 8oz plastic bottle sold as single and twin pack
Where it was distributed
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.
AlaskaAlabamaArkansasArizonaCaliforniaColoradoConnecticutDelawareFloridaGeorgiaHawaiiIowaIdahoIllinoisIndianaKansasKentuckyLouisianaMassachusettsMaryland
Questions about this recall
Is Vicks ZzzQuil Liquid Melatonin Syrup Adult sold as single and twin pack recalled?
Yes. The Procter & Gamble recalled Vicks ZzzQuil Liquid Melatonin Syrup Adult sold as single and twin pack on 12 Jul 2022. The recall is Class II and its status is Terminated. Recall number F-1537-2022.
Why was it recalled?
Acidified/Low Acid dietary supplement with no approved process.
Which lots are affected?
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 was it sold?
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.
What should I do if I have it?
Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.
What does Class II mean?
Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.
Read the official FDA notice · Source record retrieved 21 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.
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