Zero for Him
Reason Product may be contaminated with Salmonella.
Arthri-D recall
Recalled by ABH Nature's Products, Inc. · Edgewood, NY, United States
Class I — High risk. Reasonable probability of serious harm or death.
Why it was recalled
Product may be contaminated with Salmonella.
Pathogen: Salmonella
Salmonella is the most common cause of food recalls for bacteria, often in eggs, produce, nuts and spices.
The most serious food recalls: a contaminated product can cause outbreaks, hospitalisations and deaths, especially for pregnant people, young children, older adults and anyone with a weakened immune system. All bacteria & viruses recalls.
What was recalled
Arthri-D 120ct
Quantity: 10,100 bottles
Lot codes, dates and UPCs
A recall covers only these codes. Compare them with the lot number, best-by date or UPC printed on your package.
Lot# 1701-092
Where it was sold
Massachusetts Pennsylvania
FDA's distribution note: Direct to MA and PA
Do not eat it. Class I means FDA judged there is a reasonable probability of serious illness or death. If the brand, size and lot or date code on your package match, throw the product away or return it to the store for a refund, and clean any surface or container it touched. If anyone has eaten it and feels unwell, contact a doctor and mention the recall. FDA lists this recall as terminated: the company has finished removing the product, so it should no longer be on shelves - but it can still be in a freezer or pantry.
- Recalling firm
- ABH Nature's Products, Inc.
- Initiated by
- Voluntary: Firm initiated
- Recall initiated
- Jan 20, 2018
- In FDA report of
- Feb 21, 2018
- Terminated
- Jun 19, 2018
- FDA recall number
- F-0812-2018 · event 78983
- Official record
- FDA enforcement report search
Also recalled with it (1 more product)
FDA files each product of one recall action separately; these share the same FDA event.
Other recalls by ABH Nature's Products, Inc.
All Dietary Supplement manufactured and distributed by ABH…
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).