Recall · openFDA Food Enforcement

All Dietary Supplement manufactured and distributed by ABH…: FDA Recall F-0705-2020

Agency action: Jan 21, 2020Record ID: F-0705-2020
View official source ↗

What happened

Original notice title

All Dietary Supplement manufactured and distributed by ABH Nature's Products Inc., recall F-0705-2020

From the archived source record

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).

What the official notice says to do

Check the original notice for the instructions that apply to the named product, company, and affected lots.

Read the official notice →

Status and source details

Status recorded in the archive
Terminated
FDA recall classification
Class II
Recall initiated by
FDA Mandated
Report date
Feb 26, 2020
Termination date in the archive
Sep 8, 2020
Source checked
Jul 16, 2026
Record revision
fda22f4f3ae2

This is a dated record. Its current status may have changed since the source was captured. A record applies to its stated scope; it is not a safety rating for every product from a company.

Sources, dates, and coverage →

What is affected

Product
All Dietary Supplement manufactured and distributed by ABH Nature's Products Inc.
Company
ABH Nature's Products, Inc.
Lot / identifier
To be determined
Market / distribution
Nationwide and Worldwide