FDA recall record
vitafusion Fiber Well 220ct, 10 / 220 CT
FDA classification. FDA Class I, II, and III are not the same as USDA FSIS classifications and are not a cross-agency safety score.
FDA listed a termination date of February 3, 2022. openFDA does not treat this as a live recall-status tracker.
Product described in an FDA recall
vitafusion Fiber Well 220ct, 10 / 220 CT
Reason
Potential presence of a metallic mesh material in products.
Products involved
Product descriptions are copied from the FDA recall record. They are not a current catalog and are not automatically matched to WhoMadeMyFood product pages.
vitafusion Fiber Well 220ct, 10 / 220 CT
Code information listed by FDA
Product Code: 027917019840 Lot Codes: WA03087520, WA02487524, WA03086273
Distribution and firm information
Recalling firm listed by FDA: Church & Dwight Co., Inc. OGI Distribution Center
Firm location listed by FDA: North Brunswick, NJ, United States
Distribution reported by FDA: The product was distributed thru out the US and Canada, Panama, China,
Product quantity listed by FDA: 2928 Bottles
Source
Source: U.S. Food and Drug Administration (FDA), openFDA food enforcement reports.
Official FDA openFDA food enforcement record
Identifying an FDA recall record does not imply FDA endorsement of WhoMadeMyFood. Methodology.