Why it was recalled
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).
Product description
All Dietary Supplement manufactured and distributed by ABH Nature's Products Inc.
Lot numbers, UPCs & expiration codes
To be determined
Where it was sold
Nationwide and Worldwide
What to do if you have this product
- Compare the brand, size, and lot/UPC codes on your package with the codes above.
- If it matches, don't eat it. Return it to the store for a refund or throw it away.
- Wash surfaces and containers that touched the product.
- If you feel sick after eating it, contact your doctor. In an emergency call 911.
Recall details
- Recall number
- F-0705-2020
- Classification
- Class II
- Status
- Terminated
- Recall initiated
- Jan 21, 2020
- FDA report date
- Feb 26, 2020
- Quantity
- unknown
- Recall type
- FDA Mandated
- Recalling firm
- ABH Nature's Products, Inc.
Original FDA data
Every field from FDA enforcement report F-0705-2020, exactly as published.
Show all FDA fields
- City
- Edgewood
- State
- NY
- Status
- Terminated
- Country
- United States
- Event ID
- 84666
- Address
- 131 Heartland Blvd
- Code information
- To be determined
- Postal code
- 11717-8315
- Report date
- Feb 26, 2020
- Product type
- Food
- Recall number
- F-0705-2020
- Classification
- Class II
- Recalling firm
- ABH Nature's Products, Inc.
- Product quantity
- unknown
- Termination date
- Sep 8, 2020
- Reason for recall
- 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).
- Voluntary / mandated
- FDA Mandated
- Product description
- All Dietary Supplement manufactured and distributed by ABH Nature's Products Inc.
- Distribution pattern
- Nationwide and Worldwide
- Recall initiation date
- Jan 21, 2020
- Initial firm notification
- Press Release
- Center classification date
- Feb 14, 2020