All Dietary Supplement manufactured and
Recalling firm: ABH Nature's Products, Inc.
Firm ordered by consent decree to recall all products because the products were prepared, packed, or held in violation of current good manufacturing practice regulation (cGMP).
Historical recall record. This is not a new recall announcement. “Terminated” describes the FDA recall process; it does not certify that an individual package is safe. FDA termination date: Sep 8, 2020.
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FDA code information
To be determined
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Full FDA record and distribution details
Original product description
All Dietary Supplement manufactured and distributed by ABH Nature's Products Inc.
Original FDA recall reason
Firm ordered by consent decree to recall all products because the products were prepared, packed, or held in violation of current good manufacturing practice regulation (cGMP).
Recall details
- Recall number
- F-0705-2020
- Event ID
- 84666
- FDA status
- Terminated
- Initiated
- Jan 21, 2020
- Reported
- Feb 26, 2020
- Classified
- Feb 14, 2020
- Terminated
- Sep 8, 2020
- Quantity
- unknown
- Location
- Edgewood, NY, United States
- Initiation type
- FDA Mandated
- Notification
- Press Release
Where it was distributed
Nationwide and Worldwide
Data updated September 16, 2026. View official FDA data ↗
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