Why it was recalled
Potential presence of a metallic mesh material in products.
Product description
vitafusion Fiber Well 220ct, 10 / 220 CT
Lot numbers, UPCs & expiration codes
Product Code: 027917019840 Lot Codes: WA03087520, WA02487524, WA03086273
Where it was sold
The product was distributed thru out the US and Canada, Panama, China,
What to do if you have this product
- Compare the brand, size, and lot/UPC codes on your package with the codes above.
- If it matches, don't eat it. Return it to the store for a refund or throw it away.
- Wash surfaces and containers that touched the product.
- If you feel sick after eating it, contact your doctor. In an emergency call 911.
Recall details
- Recall number
- F-0462-2021
- Classification
- Class II
- Status
- Terminated
- Recall initiated
- Apr 19, 2021
- FDA report date
- May 5, 2021
- Quantity
- 2928 Bottles
- Recall type
- Voluntary: Firm initiated
- Recalling firm
- Church & Dwight Co., Inc. OGI Distribution Center
Original FDA data
Every field from FDA enforcement report F-0462-2021, exactly as published.
Show all FDA fields
- City
- North Brunswick
- State
- NJ
- Status
- Terminated
- Country
- United States
- Event ID
- 87745
- Address
- 2300 Us Highway 1
- Code information
- Product Code: 027917019840 Lot Codes: WA03087520, WA02487524, WA03086273
- Postal code
- 08902-4438
- Report date
- May 5, 2021
- Product type
- Food
- Recall number
- F-0462-2021
- Classification
- Class II
- Recalling firm
- Church & Dwight Co., Inc. OGI Distribution Center
- Product quantity
- 2928 Bottles
- Termination date
- Feb 3, 2022
- Reason for recall
- Potential presence of a metallic mesh material in products.
- Voluntary / mandated
- Voluntary: Firm initiated
- Product description
- vitafusion Fiber Well 220ct, 10 / 220 CT
- Distribution pattern
- The product was distributed thru out the US and Canada, Panama, China,
- Recall initiation date
- Apr 19, 2021
- Initial firm notification
- Letter
- Center classification date
- Apr 28, 2021