FDAFDA · Food and drugs·Recall number F-0462-2021
vitafusion Fiber Well 220ct, 10 / 220 CT
Published May 5, 2021 · Recall initiated: April 19, 2021
Status when published: Terminated — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.
What's the hazard
Potential presence of a metallic mesh material in products.
What to do
Voluntary: Firm initiated · Letter
Recall details
- Manufacturer
- Church & Dwight Co., Inc. OGI Distribution Center
- Distributor
- The product was distributed thru out the US and Canada, Panama, China,
- Lot
- Product Code: 027917019840 Lot Codes: WA03087520, WA02487524, WA03086273
- Risk classification
- Class II
- Area (FDA)
- food
- Country
- United States
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