CLASS I ONGOING Food recall · Reported 23 Sep 2026 · FDA Enforcement Report
organic moringa leaf powder recalled by Foods Alive
Foods Alive is recalling organic moringa leaf powder, distributed nationwide in the US. The recall was initiated on 26 Aug 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-1336-2026
- FDA event ID
- 99830
- Recalling firm
- Foods Alive, Angola, IN
- Classification
- Class I
- Status
- Ongoing
- Recall initiated
- 26 Aug 2026
- FDA classified
- 11 Sep 2026
- Reported
- 23 Sep 2026
- Type
- Voluntary: Firm initiated
- Customers notified by
- Reason category
- Salmonella
- Product category
- Herbal Supplements
Timeline
| 26 Aug 2026 | Recall initiated by company | |
| 11 Sep 2026 | Classified by FDA | +16 days |
| 23 Sep 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 Salmonella contamination
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
Foods Alive organic moringa leaf powder, 8oz pouch, UPC 8 91551 00092 8
Where it was distributed
Nationwide US and UAE. The recalled organic moringa leaf powder was distributed nationwide in retail stores and through online sellers including but not limited to www.foodsalive.com.
Questions about this recall
Why was it recalled?
Potential Salmonella contamination
Which lots are affected?
Freshest by 110127
Where was it sold?
Nationwide US and UAE. The recalled organic moringa leaf powder was distributed nationwide in retail stores and through online sellers including but not limited to www.foodsalive.com.
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 29 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.
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