Church & Dwight Co., Inc. OGI Distribution Center recalls vitafusion Fiber Well 220ct, 10 / 220 CT

Recalled May 5, 2021 · FDA recall F-0462-2021 · Church & Dwight Co., Inc. OGI Distribution Center

Hazard

Potential presence of a metallic mesh material in products. · FDA Class II

Units

2928 Bottles

Sold at

The product was distributed thru out the US and Canada, Panama, China,

Description

Potential presence of a metallic mesh material in products.

Product

vitafusion Fiber Well 220ct, 10 / 220 CT

Manufacturer(s)

Church & Dwight Co., Inc. OGI Distribution Center

Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →