vitafusion Melatonin 140ct, 3 Pack 140 CT vitafusion Melatonin 44ct , 3Pack 44CT
Recalled by Church & Dwight CO., INC. Ogi Distribution Center on Apr 19, 2021
Recall Summary
Church & Dwight CO., INC. Ogi Distribution Center recalled vitafusion Melatonin 140ct, 3 Pack 140 CT in a Class II action, the FDA tier for products that may cause temporary or medically reversible health effects on Apr 19, 2021.
The recall cites foreign-material contamination: "Potential presence of a metallic mesh material in products." Physical contaminants such as metal, glass, or plastic can cause choking, cuts, or dental injuries.
Distribution was limited; the FDA record lists "The product was distributed thru out the US and Canada, Panama, China,." Single-area recalls still warrant a kitchen check for anyone who shops within that footprint. The recalling firm is based in North Brunswick, NJ. The recall covers 5475 Bottles 44ct Bottles, 2081 Bottles 140 CT of product. The FDA has Terminated this recall (first reported May 5, 2021), its final lifecycle state, indicating the agency considers the corrective action resolved. The historical record remains useful for tracking a brand's recall pattern over time.
Reason for Recall
Potential presence of a metallic mesh material in products.
Product Description
vitafusion Melatonin 140ct, 3 Pack 140 CT vitafusion Melatonin 44ct , 3Pack 44CT
Distribution
The product was distributed thru out the US and Canada, Panama, China,
What Should You Do?
- 1.Check your kitchen for this product immediately.
- 2.Do not consume the recalled product.
- 3.Return the product to where you bought it for a full refund, or throw it away.
- 4.If you have experienced any health issues, contact your healthcare provider.
Terms Explained
- Class II Recall — learn what this means in food safety
- FDA Food Recall — learn what this means in food safety
Source: FDA Recalls, Market Withdrawals and Safety Alerts, 2026.