vitafusion Fiber Well 90ct — Class II food recall F-0463-2021
Terminated recall by Church & Dwight Co., Inc. OGI Distribution Center, reported 2021-05-05. Potential presence of a metallic mesh material in products.
| Recall number | F-0463-2021 |
|---|---|
| Product type | Food |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Church & Dwight Co., Inc. OGI Distribution Center, North Brunswick, NJ, United States |
| Recall initiated | 2021-04-19 |
| Classified | 2021-04-28 |
| Reported by FDA | 2021-05-05 |
| Terminated | 2022-02-03 |
| Countries outside the US | CA, CN, PA |
| Quantity | 7,782 bottles |
| UPC / GTIN / UDI-DI | 00027917018904 |
| Lot numbers | WA02187020, WA03086671, WA03087521 |
Product
vitafusion Fiber Well 90ct, 4/3 Pack 90CT
Reason for recall
Potential presence of a metallic mesh material in products.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/F-0463-2021. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.