vitafusion SleepWell 250ct / 24 / 250 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 SleepWell 250ct / 24 / 250 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: 0-27917-02524-7 Lot Codes: WA03077414
| Type | Code / value | Context |
|---|---|---|
| lot | WA03077414 | Product Code: 0-27917-02524-7 Lot Codes: WA03077414 |
Recall details
- Recall number
- F-0466-2021
- Event ID
- 87745
- FDA status
- Terminated
- Initiated
- Apr 19, 2021
- Reported
- May 5, 2021
- Classified
- Apr 28, 2021
- Terminated
- Feb 3, 2022
- Quantity
- 120 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-0466-2021
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.