Terminated Class II

Church & Dwight Co., Inc. OGI Distribution Center

Recall F-0462-2021 · North Brunswick, NJ

Product

vitafusion Fiber Well 220ct, 10 / 220 CT

Reason for recall

Potential presence of a metallic mesh material in products.

Distribution

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

Quantity affected

2928 Bottles

Recall type

Voluntary: Firm initiated

Lot / code info

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

Timeline

19 Apr 2021 initiated → 28 Apr 2021 classified → 5 May 2021 reported → 3 Feb 2022 terminated

Sourced directly from the FDA’s openFDA enforcement database. This information is for educational purposes only and does not constitute health or legal advice. FoodRecallFinder.com is not affiliated with or endorsed by the U.S. Food and Drug Administration.