Class IITerminated in FDA datasetJan 21, 2020

All Dietary Supplement manufactured and

Recalling firm: ABH Nature's Products, Inc.

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).

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ProductAll Dietary Supplement manufactured and distributed by ABH Nature's Products Inc.

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.

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

FDA source record · F-0705-2020

Data updated September 16, 2026. View official FDA data ↗

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