Reported May 5, 2021 · Terminated

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

Church & Dwight Co., Inc. OGI Distribution Center

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

What you should do

Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.

Firm contact: Church & Dwight Co., Inc. OGI Distribution Center · 2300 Us Highway 1 · North Brunswick, NJ · 08902-4438

Is this the product you have?

    • vitafusion Fiber Well 90ct
    • 4/3 Pack 90CT
Lot codes and dates
  • Product Code027917018904
  • Lot Codes
    • WA02187020
    • WA03086671
    • WA03087521
Amount recalled
7782 Bottles

This recall covers 6 products

The agency filed one notice per product. You are reading one of them; the other 5 are below.

Why it was recalled

Potential presence of a metallic mesh material in products.

This product could cause temporary or reversible health problems — stop using it.

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Where this came from

Source: U.S. Food & Drug Administration (openFDA)

Read the FDA (openFDA food enforcement) notice

Notice updated Feb 3, 2022 · Data as of Sep 19, 7:20 PM UTC

RecallNow is not a government agency. Every fact on this page is published by the FDA, USDA or CPSC and links back to their notice.