CLASS I Food recall · Reported 21 Feb 2018 · FDA Enforcement Report
Arthri-D 120ct recalled by ABH Nature's Products
ABH Nature's Products is recalling Arthri-D 120ct, distributed in Massachusetts, Pennsylvania. The recall was initiated on 20 Jan 2018 and the FDA has classified it as Class I.
Check your package
Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.
Recall details
- Recall number
- F-0812-2018
- FDA event ID
- 78983
- Recalling firm
- ABH Nature's Products, Edgewood, NY
- Brand
- Arthri-D
- Classification
- Class I
- Status
- Terminated
- Recall initiated
- 20 Jan 2018
- FDA classified
- 15 Feb 2018
- Reported
- 21 Feb 2018
- Type
- Voluntary: Firm initiated
- Customers notified by
- Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
- Reason category
- Salmonella
- Product category
- Other
Timeline
| 20 Jan 2018 | Recall initiated by company | |
| 15 Feb 2018 | Classified by FDA | +26 days |
| 21 Feb 2018 | Published in enforcement report | +6 days |
Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.
Reason for recall
Product may be contaminated with Salmonella.
Salmonella causes fever, diarrhea and abdominal cramps, usually 12 to 72 hours after eating contaminated food. Most people recover without treatment, but severe cases can need hospital care.
Product as listed by the FDA
Arthri-D 120ct
Where it was distributed
Direct to MA and PA
Questions about this recall
Is Arthri-D 120ct recalled?
Yes. ABH Nature's Products recalled Arthri-D 120ct on 20 Jan 2018. The recall is Class I and its status is Terminated. Recall number F-0812-2018.
Why was it recalled?
Product may be contaminated with Salmonella.
Which lots are affected?
Lot# 1701-092
Where was it sold?
Direct to MA and PA
What should I do if I have it?
Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.
What does Class I mean?
Class I is the most serious FDA recall category: there is a reasonable probability that using the product will cause serious health consequences or death.
Read the official FDA notice · Source record retrieved 21 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.
More recalls from ABH Nature's Products
All 3| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| Food | CLASS II | All Dietary Supplement manufactured recalled by ABH Nature's Products | ABH Nature's Products | Manufacturing (CGMP) Deviations | Nationwide |
| Food | CLASS I | Zero for Him recalled by ABH Nature's ProductsZero | ABH Nature's Products | Salmonella | MA, PA |
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