Arthri-D 120ct
Recalling firm: ABH Nature's Products, Inc.
Why it was recalled
Product may be contaminated with Salmonella.
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ProductArthri-D 120ct
FDA code information
Lot# 1701-092
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Full FDA record and distribution details
Original product description
Arthri-D 120ct
Recall details
- Recall number
- F-0812-2018
- Event ID
- 78983
- FDA status
- Terminated
- Initiated
- Jan 20, 2018
- Reported
- Feb 21, 2018
- Classified
- Feb 15, 2018
- Terminated
- Jun 19, 2018
- Quantity
- 10,100 bottles
- Location
- Edgewood, NY, United States
- Initiation type
- Voluntary: Firm initiated
- Notification
- Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Where it was distributed
Direct to MA and PA
FDA source record · F-0812-2018
Data updated September 16, 2026. View official FDA data ↗
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