Dietary Supplements (ABH Nature's) – Manufacturing Violation (2020)
Class II: A situation in which use of, or exposure to, a violative product may cause temporary or medically reversible adverse health consequences or where the probability of serious adverse health consequences is remote
Class II recall indicates potential for temporary health effects.
This AI-generated summary is provided for general informational purposes only and is derived from publicly available recall notices. It supplements but does not replace official agency classifications or safety instructions.
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
All Dietary Supplement manufactured and distributed by ABH Nature's Products Inc.
Brand
ABH Nature's Products, Inc.
Lot Codes / Batch Numbers
To be determined
Products Sold
To be determined
ABH Nature's Products, Inc. is recalling All Dietary Supplement manufactured and distributed by ABH Nature's Products Inc. due to Firm ordered by consent decree to recall all products because the products were prepared, packed, or held in violation of current good manufacturing p. This is a Class I recall, indicating a high risk of serious health consequences. Based on FDA enforcement report.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
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).
Recommended Action
Per FDA guidance
Consumers should stop using the product and contact the recalling firm or return it to the place of purchase.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticePage updated: Jan 6, 2026