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Church & Dwight Co., Inc. OGI Distribution Center
FDA recall F-0462-2021 · Class II · reported 2021-05-05 · Terminated
- Product
- vitafusion Fiber Well 220ct, 10 / 220 CT
- Reason
- Potential presence of a metallic mesh material in products.
- Quantity
- 2928 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: 027917019840 Lot Codes: WA03087520, WA02487524, WA03086273
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.