FDA recall record
All Dietary Supplement manufactured and distributed by ABH Nature's Products Inc.
FDA classification. FDA Class I, II, and III are not the same as USDA FSIS classifications and are not a cross-agency safety score.
FDA listed a termination date of September 8, 2020. openFDA does not treat this as a live recall-status tracker.
Product described in an FDA recall
All Dietary Supplement manufactured and distributed by ABH Nature's Products Inc.
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).
Products involved
Product descriptions are copied from the FDA recall record. They are not a current catalog and are not automatically matched to WhoMadeMyFood product pages.
All Dietary Supplement manufactured and distributed by ABH Nature's Products Inc.
Code information listed by FDA
To be determined
Distribution and firm information
Recalling firm listed by FDA: ABH Nature's Products, Inc.
Firm location listed by FDA: Edgewood, NY, United States
Distribution reported by FDA: Nationwide and Worldwide
Product quantity listed by FDA: unknown
Source
Source: U.S. Food and Drug Administration (FDA), openFDA food enforcement reports.
Official FDA openFDA food enforcement record
Identifying an FDA recall record does not imply FDA endorsement of WhoMadeMyFood. Methodology.