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RECALL RECORD — CLASS IIRecall closedF-0464-2021/FDA enforcement
Church & Dwight Co., INC. Ogi Distribution Center·Food·Apr 19, 2021

Vitafusion Melatonin 140ct, 3 Pack 140 Ct Vitafusion Melatonin 44ct, 3pack 44ct

What you need to know

Class II

  • What happened

    Potential presence of a metallic mesh material in products.

  • 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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Match before you discard

Product identification

Source: FDA FOOD

Brand nameChurch & Dwight Co., INC. Ogi Distribution Center
Recalling firmChurch & Dwight Co., INC. Ogi Distribution CenterNorth Brunswick, NJ, United States
UPC / barcodes
0 27917 02671 80 27917 28011 0
Lot / date codes
  • Product Code: 0-27917-02671-8 Lot Codes: WA03076990, WA03077852, WA02608988 Product Code: 0-27917-28011-0 Lot Codes: WA03076270
Distribution area

The product was distributed thru out the US and Canada, Panama, China,

Canada, China

Quantity affected5475 Bottles 44ct Bottles, 2081 Bottles 140 CT
Recall initiationFDA report date: May 5, 2021
FDA recall numberF-0464-2021

Beyond the headline

The recall, in context

Church & Dwight Co., INC. Ogi Distribution Center initiated this food recall on April 19, 2021. The FDA enforcement report states: Potential presence of a metallic mesh material in products. The FDA report lists distribution as: The product was distributed thru out the US and Canada, Panama, China,.

The FDA enforcement report describes the reason as: Potential presence of a metallic mesh material in products.

Vitafusion Melatonin 140ct, 3 Pack 140 Ct Vitafusion Melatonin 44ct, 3pack 44ct was made or distributed by Church & Dwight Co., INC. Ogi Distribution Center in North Brunswick, NJ, United States. This page reflects FDA report F-0464-2021, dated May 5, 2021.

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. 1

    Stop using it

    Do not eat, drink or take the affected product.

  2. 2

    Check the codes

    Compare the UPC and lot code against the table above.

  3. 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

  1. 1Stop using or eating the product and keep it away from children and pets.
  2. 2Check the UPC and lot/date codes on this page and follow the official recall notice for disposal or return.
  3. 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

What is the Vitafusion Melatonin 140ct, 3 Pack 140 Ct Vitafusion Melatonin 44ct, 3pack 44ct recall?

Church & Dwight Co., INC. Ogi Distribution Center recalled Vitafusion Melatonin 140ct, 3 Pack 140 Ct Vitafusion Melatonin 44ct, 3pack 44ct in an FDA Class II enforcement action reported as F-0464-2021. Potential presence of a metallic mesh material in products.

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 Church & Dwight Co., INC. Ogi Distribution Center 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-0464-2021. 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.

Official source

Brand history

More recalls by Church & Dwight Co., INC. Ogi Distribution Center

View brand
Class II·

Church & Dwight Co., INC. Ogi Distribution Center

Vitafusion Fiber Well 220ct, 10 / 220 Ct

Potential presence of a metallic mesh material in products.

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Class II·

Church & Dwight Co., INC. Ogi Distribution Center

Vitafusion Sleepwell 250ct / 24 / 250 Ct

Potential presence of a metallic mesh material in products.

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Record last synced from official openFDA enforcement data on November 14, 2026. Source record: official FDA notice.