FDAClass I · Food · Recall H-1180-2026 · Recalled July 29, 2026

Organic Moringa Powder recall — Green Jeeva LLC

Agency report date: July 29, 2026.

1. Compare your item

This notice names a product; your particular item is not yet verified. Compare every applicable model, serial, lot, production-date or model-year boundary below.

Product named: Organic Moringa Powder
Company / brand: Green Jeeva
Lot / serial / date codes: lot: 25/08001 Expiration date: 02-11-2028
Distribution: Product was distributed to 4 different consignees who have used the ingredient for further processing and distribution.

Agency product description and boundaries

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

Still to verify: match the label on your item with the full official notice, including any exclusions, tables and photos. Some identifiers appear only on the agency website and are absent from this data feed. A missing field does not mean all versions are affected.

If your lot or date falls outside a stated range, this notice has not established that your item is affected. This is not a finding about other recalls or product safety.

2. Agency hazard and consumer action

FDA reports: Moringa Powder ingredient positive for salmonella

No consumer remedy instructions are supplied in this record. Check the official notice and listed company contact for the agency’s current instructions.

Class I: most serious — reasonable probability of serious health consequences or death.

Affected product: Organic Moringa Powder

3. Open the official notice or contact

View the official FDA enforcement record (openFDA) ↗

Official recall ID: H-1180-2026
Brand: Green Jeeva
Classification: Class I
Units affected: 2,490 kg
Recall status: Ongoing
Initiated: Voluntary: Firm initiated

Affected products

Organic Moringa Powder

Companies & origin

Recalling firm location: Cerritos, CA, United States
Firm address: 16200 Carmenita Rd Ste A, N/A, 90703-2255

Identifying details (verbatim from the notice)

Product codes / lots: lot: 25/08001 Expiration date: 02-11-2028
Distribution: Product was distributed to 4 different consignees who have used the ingredient for further processing and distribution.
Firm notified the public via: E-Mail
FDA event ID: 99387
Recall initiated: July 8, 2026
FDA classified: July 21, 2026
FDA report date: July 29, 2026

Verify with the official sources:

CPSC — consumer products ↗ (aggregated here)
NHTSA — vehicles, car seats, tires ↗ (aggregated here; use NHTSA's VIN lookup to check a specific vehicle)
FDA — food, drugs, medical devices ↗ (aggregated here)
USDA FSIS — meat, poultry & processed egg products ↗ (not aggregated here)
Recalls.gov — the U.S. government’s all-agency portal ↗

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Source: U.S. Food & Drug Administration. Agency excerpts come from the public data feed and may omit tables or later changes; the linked government source is authoritative. Source last checked September 7, 2026 at 6:00 AM UTC. Record retrieved September 7, 2026 at 6:00 AM UTC.

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