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

Recall date

April 19, 2021

Source

U.S. Food & Drug Administration (FDA) — enforcement report

Recall number

F-0462-2021

FDA classification

Class II

Brand / firm

Church & Dwight Co., Inc. OGI Distribution Center

Sold / distributed

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

Why it was recalled

Potential presence of a metallic mesh material in products.

Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.

What was recalled

vitafusion Fiber Well 220ct, 10 / 220 CT