FDA Recall United States TerminatedTerminated: June 19, 2018Historical recordClass I
ABH Nature's Products, Inc.
- Product
- Zero for Him 150 count
- Published
- February 21, 2018
- Distribution
- Direct to MA and PA
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). - F-0705-2020
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).
- - Recall initiated
- - Reported by source
- - Recall terminated
| 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 TerminatedTerminated: June 19, 2018Historical recordClass I
ABH Nature's Products, Inc.
- Product
- Arthri-D 120ct
- Published
- February 21, 2018
- Distribution
- Direct to MA and PA
Where this information comes from
View FDA enforcement record -- the specific openFDA record this summary was built from.
This record comes from FDA's Enforcement Report database. Not every Enforcement Report record has a separate FDA.gov recall-announcement page.
FDA Enforcement Reports -- FDA's general, official recall and enforcement information. See FDA Enforcement Reports versus recall announcements for how that database differs from a press-release-style announcement.
New to reading a recall record? See how to read an FDA recall record and what recall statuses mean.
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?
FDA classifies this recall as Class II. See how to read an FDA recall record (linked above) for what each classification level means.
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 responsible agency's published instructions, linked below -- recall guidance is set by that agency, not by Public Health Trace.
Official guidance and record verification
Public Health Trace does not provide medical advice -- review the linked official source below for current, authoritative information.
How to interpret this historical record
This record is preserved as published by FDA, as of September 8, 2020.
Status as reported: Terminated.
This page does not imply a current danger or a current consumer instruction -- review the official source for the most current information.
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.