ABH Arthri-D Recall: Salmonella Contamination Risk
ABH Nature's Products recalls Arthri-D 120ct due to potential Salmonella contamination. Check your lot number and distribution area for details.
Stop using this now
Product may be contaminated with Salmonella.
Contact the company
What happened, in plain English
ABH Nature's Products, Inc. is recalling Arthri-D 120ct dietary supplements because they may be contaminated with Salmonella. The recall covers 10,100 bottles distributed directly to customers in Massachusetts and Pennsylvania. This is a Class I recall, indicating the highest risk of adverse health consequences. Read more at govinfonow.com/recall/19739-abh-arthri-d-recall-salmonella-contamination-risk.
Source Summary by GovInfoNow · govinfonow.com/recall/19739-abh-arthri-d-recall-salmonella-contamination-risk · Updated October 11, 2026 · FDA enforcement record: FDA #F-0812-2018
Cite this page
“ABH Arthri-D Recall: Salmonella Contamination Risk.” GovInfoNow, updated October 11, 2026. https://govinfonow.com/recall/19739-abh-arthri-d-recall-salmonella-contamination-risk. Based on FDA recall #F-0812-2018 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-0812-2018%22&limit=1).
Why it’s dangerous
Salmonella is a bacterium that can cause foodborne illness. Ingestion of contaminated supplements can lead to symptoms such as fever, diarrhea, abdominal cramps, and vomiting, which can be severe or life-threatening for vulnerable populations.
Who’s affected
Consumers who purchased Arthri-D 120ct supplements directly from ABH Nature's Products, Inc. in Massachusetts or Pennsylvania are affected. Individuals with weakened immune systems, the elderly, and young children are at higher risk for serious infection if contaminated.
How to tell if you have this one
Check if you have Arthri-D 120ct bottles manufactured by ABH Nature's Products, Inc. Look specifically for Lot# 1701-092 on the packaging. The product was distributed directly to consumers in Massachusetts and Pennsylvania.
- Brand
ABH Nature's Products- Category
Food
All 2 products in this recall
FDA lists each product line separately under one recall event. Check your product description, lot or code numbers against each row. Every row shares the hazard and remedy on this page.
- Classification
Class I- Status
Terminated- Distribution
Direct to MA and PA
| Recall number | Product, codes & lots | Quantity |
|---|---|---|
| F-0812-2018 | Arthri-D 120ct; Lot# 1701-092 | 10,100 bottles |
| F-0813-2018 | Zero for Him 150 count; Lot#1710638B | 1,137 bottles |
What to do — step by step
Stop using the product
Do not consume any Arthri-D 120ct supplements from the recalled lot due to Salmonella risk.
Check your lot number
Verify if your bottle has Lot# 1701-092 to confirm if it is part of this specific recall.
Contact the manufacturer
Reach out to ABH Nature's Products, Inc. for further instructions on disposal or refund since no specific remedy was listed in the record.
Where it went and when
Where it was distributed
Distributed in Massachusetts and Pennsylvania.
FDA distribution: “Direct to MA and PA” States read from FDA’s own wording; “not listed” means the notice does not name it.
States: Massachusetts, Pennsylvania.
Recall timeline
FDA terminated this recall 5 months after the firm started it.
- Firm started the recall
- FDA classified it Class I
- Published in FDA’s Enforcement Report
- FDA terminated the recall
Dates from the agency record only; steps without a date are left out.
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Where this comes from
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
- Official source: FDA Recall #F-0812-2018 (January 20, 2018) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-0812-2018 to see it in context.
- Plain-language summary written by qwen3.6:35b-a3b on October 11, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
- GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.