vitafusion Fiber Well 90ct, 4/3 Pack 90CT

Recall map → All recalls → F-0463-2021

vitafusion Fiber Well 90ct, 4/3 Pack 90CT Church & Dwight Co., Inc. OGI Distribution Center · reported 2021-05-05

Terminated This recall has been closed out by the agency.

Reason for recall: Potential presence of a metallic mesh material in products.
Classification: Class II
Recall initiated: 2021-04-19
Reported by the agency: 2021-05-05
Closed out (terminated): 2022-02-03
Recalling firm: Church & Dwight Co., Inc. OGI Distribution Center
North Brunswick, NJ
United States
This is the firm that issued the recall — commonly a distributor or processor. It is not the origin of contamination.
Distribution (the agency's own words): The product was distributed thru out the US and Canada, Panama, China,
States we parsed from that text: could not be parsed
No state list could be read from the agency's text. Absence here is not evidence the product stayed put.
Food category: uncategorised
Assigned by a reviewed keyword rulebook over the product description, not by the agency.
Recall type: Voluntary: Firm initiated
Recall number: F-0463-2021

This page reproduces a record published by the US Food and Drug Administration. It is not real-time: recalls typically appear in FDA's Enforcement Report weeks after they begin — a median of 40 days, see publication lag. For current food safety information consult FDA and USDA FSIS directly.