vitafusion Fiber Well recall

Recalled by Church & Dwight Co., Inc. OGI Distribution Center · North Brunswick, NJ, United States

Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.

Why it was recalled

Potential presence of a metallic mesh material in products.

See the recall's own reason text for the specifics. All other reasons recalls.

What was recalled

vitafusion Fiber Well 220ct, 10 / 220 CT

Quantity: 2928 Bottles

Lot codes, dates and UPCs

A recall covers only these codes. Compare them with the lot number, best-by date or UPC printed on your package.

Product Code: 027917019840 Lot Codes: WA03087520, WA02487524, WA03086273

Where it was sold

FDA's distribution note: The product was distributed thru out the US and Canada, Panama, China,

Check the codes, then return or discard. Class II means eating it may cause temporary or reversible health problems. If your package matches the recalled codes, do not eat it - return it to the store or throw it away. FDA lists this recall as terminated: the company has finished removing the product, so it should no longer be on shelves - but it can still be in a freezer or pantry.

Recalling firm: Church & Dwight Co., Inc. OGI Distribution Center
Initiated by: Voluntary: Firm initiated
Recall initiated: Apr 19, 2021
In FDA report of: May 5, 2021
Terminated: Feb 3, 2022
FDA recall number: F-0462-2021 · event 87745
Official record: FDA enforcement report search

Also recalled with it (5 more products)

FDA files each product of one recall action separately; these share the same FDA event.

Class II · Moderate risk Terminated Apr 19, 2021