CLASS I Food recall · Reported 25 Feb 2026 · FDA Enforcement Report
Why Not Natural Moringa Capsules bottle marked recalled by Art Monkey
Art Monkey is recalling Why Not Natural Moringa Capsules bottle marked, distributed nationwide in the US. The recall was initiated on 28 Jan 2026 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
- H-0510-2026
- FDA event ID
- 98367
- Recalling firm
- Art Monkey, Houston, TX
- Brand
- Why Not
- Classification
- Class I
- Status
- Terminated
- Recall initiated
- 28 Jan 2026
- FDA classified
- 13 Feb 2026
- Reported
- 25 Feb 2026
- 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
- Herbal Supplements
Timeline
| 28 Jan 2026 | Recall initiated by company | |
| 13 Feb 2026 | Classified by FDA | +16 days |
| 25 Feb 2026 | Published in enforcement report | +12 days |
Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.
Reason for recall
Potential to 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
Why Not Natural Moringa Capsules 120 capsule bottle marked with lot # A25G051 on the bottom and with an expiration date of 07/2028 stamped on the bottom.
Where it was distributed
Nationwide
Questions about this recall
Why was it recalled?
Potential to be contaminated with Salmonella
Which lots are affected?
lot # A25G051
Where was it sold?
Nationwide
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 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.
Other Herbal Supplements recalls
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|---|---|---|---|---|---|
| Food | CLASS III | American Ginsengs recalled by Kwok Shing | Kwok Shing | Other | CA |
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