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Church & Dwight Co., Inc. OGI Distribution Center
FDA recall F-0466-2021 · Class II · reported 2021-05-05 · Terminated
- Product
- vitafusion SleepWell 250ct / 24 / 250 CT
- Reason
- Potential presence of a metallic mesh material in products.
- Quantity
- 120 Bottles
- Distribution
- The product was distributed thru out the US and Canada, Panama, China,
- Firm location
- NJ, United States
- Initiated
- Voluntary: Firm initiated
- First notice
- Letter
- Recall started
- 2021-04-19
- Terminated
- 2022-02-03
- Code info
- Product Code: 0-27917-02524-7 Lot Codes: WA03077414
Source: U.S. Food and Drug Administration, openFDA Food Enforcement database (openFDA Food Enforcement, imported 2026-09). The FDA does not validate openFDA data for completeness or accuracy. This is a record of an enforcement action, not safety advice.