vitafusion MultiVites 150ct
Recalling firm: Church & Dwight Co., Inc. OGI Distribution Center
Why it was recalled
Potential presence of a metallic mesh material in products.
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Productvitafusion MultiVites 150ct,
FDA code information
Product Code: 027917019192 Lot Codes: WA03044959
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Full FDA record and distribution details
Original product description
vitafusion MultiVites 150ct,
Extracted codes and context
| Type | Code / value | Context |
|---|---|---|
| lot | WA03044959 | Product Code: 027917019192 Lot Codes: WA03044959 |
Recall details
- Recall number
- F-0461-2021
- Event ID
- 87745
- FDA status
- Terminated
- Initiated
- Apr 19, 2021
- Reported
- May 5, 2021
- Classified
- Apr 28, 2021
- Terminated
- Feb 3, 2022
- Quantity
- 683 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-0461-2021
Data updated September 16, 2026. View official FDA data ↗
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