Recalls / Class II
Class IIF-0466-2021
Product
vitafusion SleepWell 250ct / 24 / 250 CT
- Type
- Food
- Affected lot / code info
- Product Code: 0-27917-02524-7 Lot Codes: WA03077414
- Quantity
- 120 Bottles
Why it was recalled
Potential presence of a metallic mesh material in products.
Recalling firm
- Firm
- Church & Dwight Co., Inc. OGI Distribution Center
- Notification channel
- Letter
- Type
- Voluntary: Firm initiated
- Address
- 2300 Us Highway 1, N/A, North Brunswick, New Jersey 08902-4438
Distribution
- Distribution pattern
- The product was distributed thru out the US and Canada, Panama, China,
Timeline
- Recall initiated
- 2021-04-19
- FDA classified
- 2021-04-28
- Posted by FDA
- 2021-05-05
- Terminated
- 2022-02-03
- Status
- Terminated
Source: openFDA Food Enforcement endpoint. Recall record F-0466-2021. The FDA issues recall classifications as health-hazard assessments, not legal findings.