CLASS I ONGOING Food recall · Reported 29 Jul 2026 · FDA Enforcement Report

Organic Moringa Powder recalled by Green Jeeva

Green Jeeva is recalling Organic Moringa Powder. The recall was initiated on 8 Jul 2026 and the FDA has classified it as Class I.

Check your package

Lot, batch or date codeslot: 25/08001 Expiration date: 02-11-2028
Quantity recalled2,490 kg

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-1180-2026
FDA event ID
99387
Recalling firm
Green Jeeva, Cerritos, CA
Classification
Class I
Status
Ongoing
Recall initiated
8 Jul 2026
FDA classified
21 Jul 2026
Reported
29 Jul 2026
Type
Voluntary: Firm initiated
Customers notified by
E-Mail
Reason category
Salmonella
Product category
Herbal Supplements

Timeline

8 Jul 2026Recall initiated by company
21 Jul 2026Classified by FDA+13 days
29 Jul 2026Published 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

Moringa Powder ingredient positive for 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

Organic Moringa Powder; 15kg/bag (bulk); Product code: GJ96

Where it was distributed

Product was distributed to 4 different consignees who have used the ingredient for further processing and distribution.

Questions about this recall

Why was it recalled?

Moringa Powder ingredient positive for salmonella

Which lots are affected?

lot: 25/08001 Expiration date: 02-11-2028

Where was it sold?

Product was distributed to 4 different consignees who have used the ingredient for further processing and distribution.

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.

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