vitafusion Fiber Well 90ct, 4/3 Pack 90CT
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 Fiber Well 90ct, 4/3 Pack 90CT
FDA code information
Product Code: 027917018904 Lot Codes: WA02187020, WA03086671, WA03087521
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Full FDA record and distribution details
Original product description
vitafusion Fiber Well 90ct, 4/3 Pack 90CT
Extracted codes and context
| Type | Code / value | Context |
|---|---|---|
| lot | WA02187020 | Product Code: 027917018904 Lot Codes: WA02187020, WA03086671, WA03087521 |
| lot | WA03086671 | Product Code: 027917018904 Lot Codes: WA02187020, WA03086671, WA03087521 |
| lot | WA03087521 | Product Code: 027917018904 Lot Codes: WA02187020, WA03086671, WA03087521 |
Recall details
- Recall number
- F-0463-2021
- Event ID
- 87745
- FDA status
- Terminated
- Initiated
- Apr 19, 2021
- Reported
- May 5, 2021
- Classified
- Apr 28, 2021
- Terminated
- Feb 3, 2022
- Quantity
- 7782 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-0463-2021
Data updated September 16, 2026. View official FDA data ↗
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