Reported May 5, 2021 · Terminated
vitafusion Fiber Well 220ct, 10 / 220 CT
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 220ct10 / 220 CT
- Lot codes and dates
- Product Code027917019840
- Lot Codes
WA03087520WA02487524WA03086273
- Amount recalled
- 2928 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.
Want the full recall guide?
The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.
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