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
ABH Nature's Products, Inc. Recall: Product may be contaminated with Salmonella. - F-0813-2018
United States
TerminatedClass I
- Company
- ABH Nature's Products, Inc.
- Product
- Zero for Him 150 count
- Recall date
- January 20, 2018
- Terminated
- June 19, 2018
- Source
- FDA
Reason for recall
Product may be contaminated with Salmonella.
- - Recall initiated
- - Reported by source
- - Recall terminated
| Product description | UPC | Quantity | Lot / code information |
|---|---|---|---|
| Zero for Him 150 count | Not published in this source record | 1,137 bottles | Lot#1710638B |
Distribution
- Direct to MA and PA
Official source record
- Agency
- FDA
- Dataset
- FDA Food Enforcement (Recalls)
- Recall number
- F-0813-2018
- Event ID
- 78983
- Status
- Terminated
- Classification
- Class I
- Company
- ABH Nature's Products, Inc.
- Product description
- Zero for Him 150 count
- Quantity
- 1,137 bottles
- Reason
- Product may be contaminated with Salmonella.
- Recall initiation date
- January 20, 2018
- Report date
- February 21, 2018
- Classification date
- Not published in this source record
- Termination date
- June 19, 2018
- Distribution pattern
- Direct to MA and PA
- UPC, lot, and code information
- Lot#1710638B
- Voluntary or mandated
- Voluntary: Firm initiated
- Initial notification method
- Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
- Source last updated
- Not tracked separately from the Public Health Trace retrieval date below
- Public Health Trace retrieval date
Other products recalled under this same event
This recall shares FDA event ID 78983 with 1 other product entry in Public Health Trace.
Responsible company: ABH Nature's Products, Inc.
Other recalls from ABH Nature's Products, Inc.
FDA Recall United States TerminatedTerminated: September 8, 2020Historical recordClass II
ABH Nature's Products, Inc.
- Product
- All Dietary Supplement manufactured and distributed by ABH N…
- Published
- February 26, 2020
- Distribution
- Nationwide
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
A map highlighting the states named in the source's distribution description.
Shading reflects state-level totals only, as published by the source. It does not imply county-level or point-level precision.
| State | Distributed |
|---|---|
| Massachusetts | 1 |
| Pennsylvania | 1 |
States shown are extracted from the source's free-text distribution description above; a narrative description (e.g. "distributed nationwide") may not list individual states to extract.
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 I mean?
FDA classifies this recall as Class I. 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 June 19, 2018.
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.