Vicks Zzzquil Liquid Melatonin Syrup Adult 8oz Plastic Bottle Sold as Single and Twin Pack
What you need to know
Class II
What happened
Acidified/Low Acid dietary supplement with no approved process.
Health risk
The product may cause temporary or medically reversible health consequences, or the probability of serious harm is remote. A safety issue that does not fit the standard pathogen, allergen, chemical or quality categories.
Action required
Check the identifying codes below and stop using the product. Return it to the retailer for a refund or dispose of it safely, following the recall notice.
Recall closed · classified by the FDADistribution not listedMore food
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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.
United States
Quantity affected
90, 522 cases
Recall initiation
FDA report date: August 10, 2022
FDA recall number
F-1537-2022
Beyond the headline
The recall, in context
The Procter & Gamble Company initiated this food recall on July 12, 2022. The FDA enforcement report states: Acidified/Low Acid dietary supplement with no approved process. The FDA report lists distribution as: 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.
The FDA enforcement report describes the reason as: Acidified/Low Acid dietary supplement with no approved process.
Vicks Zzzquil Liquid Melatonin Syrup Adult 8oz Plastic Bottle Sold as Single and Twin Pack was made or distributed by The Procter & Gamble Company in Cincinnati, OH, United States. This page reflects FDA report F-1537-2022, dated August 10, 2022.
Why this is a Class II recall
Class II means the product may cause temporary or medically reversible health consequences, or the probability of serious harm is remote. In this recall, a safety issue that does not fit the standard pathogen, allergen, chemical or quality categories.
FDA definition
The product may cause temporary or medically reversible health consequences, or the probability of serious harm is remote.
What to do now
1
Stop using it
Do not eat, drink or take the affected product.
2
Check the codes
Compare the UPC and lot code against the table above.
3
Return or discard
Contact the retailer or recalling firm about a refund, and dispose of the product safely.
Consumer safety guide
Product safety recall
Symptoms to watch for
The official enforcement report describes the specific risk. Follow the recall notice, check the product codes and do not use a product that may be affected.
Higher-risk groups
Children, pregnant people, older adults and people with weakened immune systems should take extra care when a product's safety is uncertain.
What to do now
1Stop using or eating the product and keep it away from children and pets.
2Check the UPC and lot/date codes on this page and follow the official recall notice for disposal or return.
3Seek medical advice if anyone develops severe or worrying symptoms after exposure.
Read the official source record for the specific hazard and instructions.
This is general consumer safety information, not medical advice or a diagnosis. Follow the official recall notice and contact a healthcare professional if you have concerns about exposure or symptoms.
Frequently asked
Questions about this recall
4 answers
What is the Vicks Zzzquil Liquid Melatonin Syrup Adult 8oz Plastic Bottle Sold as Single and Twin Pack recall?
The Procter & Gamble Company recalled Vicks Zzzquil Liquid Melatonin Syrup Adult 8oz Plastic Bottle Sold as Single and Twin Pack in an FDA Class II enforcement action reported as F-1537-2022. Acidified/Low Acid dietary supplement with no approved process.
What should I do if I bought this product?
Check the identifying codes below and stop using the product. Return it to the retailer for a refund or dispose of it safely, following the recall notice. Stop using or eating the product and keep it away from children and pets. Check the UPC and lot/date codes on this page and follow the official recall notice for disposal or return. Seek medical advice if anyone develops severe or worrying symptoms after exposure.
Is the The Procter & Gamble Company recall still active?
The FDA lists this recall as recall closed. It remains relevant if you still have the affected product or need to identify a historical recall.
Where can I verify this recall?
This page is normalized from the openFDA enforcement record F-1537-2022. You can verify it directly using the official source link on this page. VerifyRecall updates its index from public FDA enforcement data and does not replace advice from the FDA, the recalling firm or a healthcare professional.
Verify before you act.
VerifyRecall is independent and not affiliated with the FDA. Always confirm the latest status on the official source record.