CLASS I ONGOING Food recall · Reported 15 Jul 2026 · FDA Enforcement Report
Organic Moringa Leaf Powder recalled by Trafa Pharmaceutical
Trafa Pharmaceutical is recalling Trafa Pharmaceuticals Inc. brand Organic Moringa Leaf Powder, distributed in New York. The recall was initiated on 24 Jun 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-1144-2026
- FDA event ID
- 99314
- Recalling firm
- Trafa Pharmaceutical, Chicopee, MA
- Brand
- Pharmaceuticals Inc
- Classification
- Class I
- Status
- Ongoing
- Recall initiated
- 24 Jun 2026
- FDA classified
- 7 Jul 2026
- Reported
- 15 Jul 2026
- Type
- Voluntary: Firm initiated
- Customers notified by
- Reason category
- Salmonella
- Product category
- Herbal Supplements
Timeline
| 24 Jun 2026 | Recall initiated by company | |
| 7 Jul 2026 | Classified by FDA | +13 days |
| 15 Jul 2026 | Published in enforcement report | +8 days |
Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.
Reason for recall
Potential contamination 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
Trafa Pharmaceuticals Inc. brand ORGANIC MORINGA LEAF POWDER; NET WEIGHT: 15 KGS; packaged in brown paper bags with a white label
Where it was distributed
NY
Questions about this recall
Is Organic Moringa Leaf Powder recalled?
Yes. Trafa Pharmaceutical recalled Organic Moringa Leaf Powder on 24 Jun 2026. The recall is Class I and its status is Ongoing. Recall number H-1144-2026.
Why was it recalled?
Potential contamination with Salmonella
Which lots are affected?
BATCH #TRF-2025050801 MAN. DATE: 2025-05-08 RESTEST. DATE: 2028-05-07
Where was it sold?
NY
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.
Other Herbal Supplements recalls
All 509| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| Food | CLASS I | Lacnola; Small recalled by The Hampton Grocer | The Hampton Grocer | Salmonella | Nationwide |
| Food | ANNOUNCED | Moringa Leaf Powder recalled by Foods AliveFoods Alive | Foods Alive | Salmonella | Nationwide |
| Food | CLASS II | A-L Complex Herbal Supplement May Contain Nuts recalledByron | Byron White Formulas | Undeclared Tree Nuts | 50 states |
| Food | CLASS II | A-P Herbal Supplement May Contain Nuts recalled by Byron White FormulasByron | Byron White Formulas | Undeclared Tree Nuts | 50 states |
| Food | CLASS II | A-fng Herbal Supplement May Contain Nuts recalledByron | Byron White Formulas | Undeclared Tree Nuts | 50 states |