vitafusion Fiber Well 220ct, 10 / 220 CT
Recalling firm: Church & Dwight Co., Inc. OGI Distribution Center
Why it was recalled
Potential presence of a metallic mesh material in products.
The exact product
vitafusion Fiber Well 220ct, 10 / 220 CT
Check the codes
Compare these FDA-provided codes, lot numbers or dates with the product you have.
Match the product, size and code together. A similar name alone does not identify your batch.
Original FDA code information
Product Code: 027917019840 Lot Codes: WA03087520, WA02487524, WA03086273
| Type | Code / value | Context |
|---|---|---|
| lot | WA02487524 | Product Code: 027917019840 Lot Codes: WA03087520, WA02487524, WA03086273 |
| lot | WA03086273 | Product Code: 027917019840 Lot Codes: WA03087520, WA02487524, WA03086273 |
| lot | WA03087520 | Product Code: 027917019840 Lot Codes: WA03087520, WA02487524, WA03086273 |
Recall details
- Recall number
- F-0462-2021
- Event ID
- 87745
- FDA status
- Terminated
- Initiated
- Apr 19, 2021
- Reported
- May 5, 2021
- Classified
- Apr 28, 2021
- Terminated
- Feb 3, 2022
- Quantity
- 2928 Bottles
- Location
- North Brunswick, NJ, United States
- Initiation type
- Voluntary: Firm initiated
- Notification
- Letter
Where it was distributed
The product was distributed thru out the US and Canada, Panama, China,
FDA source record · F-0462-2021
Data updated September 16, 2026. View official FDA data ↗
A missing code match is not a guarantee of safety. Follow official FDA and manufacturer guidance.