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ABH Nature's Products, Inc. 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).

United States

TerminatedClass II

Company
ABH Nature's Products, Inc.
Product
All Dietary Supplement manufactured and distributed by ABH N…
Recall date
January 21, 2020
Terminated
September 8, 2020
Source
FDA

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).

  1. - Recall initiated
  2. - Reported by source
  3. - Recall terminated
Recalled products
Product description UPC Quantity Lot / code information
All Dietary Supplement manufactured and distributed by ABH Nature's Products Inc. Not published in this source record unknown To be determined

Distribution

  • Nationwide and Worldwide

Official source record

Agency
FDA
Dataset
FDA Food Enforcement (Recalls)
Recall number
F-0705-2020
Event ID
84666
Status
Terminated
Classification
Class II
Company
ABH Nature's Products, Inc.
Product description
All Dietary Supplement manufactured and distributed by ABH Nature's Products Inc.
Quantity
unknown
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).
Recall initiation date
January 21, 2020
Report date
February 26, 2020
Classification date
Not published in this source record
Termination date
September 8, 2020
Distribution pattern
Nationwide and Worldwide
UPC, lot, and code information
To be determined
Voluntary or mandated
FDA Mandated
Initial notification method
Press Release
Source last updated
Not tracked separately from the Public Health Trace retrieval date below
Public Health Trace retrieval date

Responsible company: ABH Nature's Products, Inc.

Other recalls from ABH Nature's Products, Inc.

FDA Recall United States Terminated Historical recordClass I

ABH Nature's Products, Inc.

Product
Zero for Him 150 count
Published
February 21, 2018
Distribution
Direct to MA and PA

View recall →

FDA Recall United States Terminated Historical recordClass I

ABH Nature's Products, Inc.

Product
Arthri-D 120ct
Published
February 21, 2018
Distribution
Direct to MA and PA

View recall →

Where this information comes from

View FDA enforcement record -- the specific openFDA record this summary was built from.

No separate FDA public notice was found for this enforcement record. The information below comes from FDA's Recall Enterprise System through openFDA.

FDA Enforcement Reports -- FDA's general, official recall and enforcement information.

Technical source data

View raw source data -- the machine-readable record this page's information was built from.

Retrieved by Public Health Trace:

Frequently asked questions

What does a Class II mean?

A situation in which use of or exposure to a product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote.

Is this recall still active?

According to FDA, this recall's status is "Terminated." Always confirm the current status using the source links below, since status can change after Public Health Trace last retrieved this record.

What should I do if I have this product?

Follow the instructions published by the responsible agency (see the source links below) -- recall guidance (e.g. dispose of the product, return it for a refund, or check for a specific lot number) varies by recall and is set by that agency, not by Public Health Trace.

Where can I find more official information?

The source links below, published by FDA, are the authoritative record for this recall, including any updates issued after this summary was retrieved.

This summary is based on the official source record referenced above. Public Health Trace does not state that any company or product is unsafe beyond what the official source has published. Read the full medical disclaimer.