Green Jeeva LLC Recalls Organic Moringa Powder
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Green Jeeva LLC is recalling 2,490 kg of Organic Moringa Powder after the ingredient tested positive for salmonella.
What this FDA recall tells you, and what most readers miss
This notice was issued by FDA on August 11, 2026 and geographically references United States. Its severity classification of "high" signals how the issuing agency weighs the risk of harm if no action is taken - "critical" and "high" tier alerts typically carry direct consumer actions, while "medium" and "low" tend toward informational guidance or monitoring advisories. The category it belongs to - FDA Recalls - determines the consumer-protection framework behind it, which shapes what remedies (refunds, replacements, repairs, or the recall itself) are available to affected consumers and which agency holds statutory responsibility for enforcement.
Most readers skim a notice like this, check whether they are personally affected, and move on. The more useful lens is to verify its scope, source, and timestamp, then compare related notices without assuming that one record proves a broader trend.
Areazine pairs this record with the original agency URL so you can check the primary source before acting. Its related labels are recall, product-safety, fda, food.
What Happened
Green Jeeva LLC has initiated a voluntary recall of Organic Moringa Powder because the ingredient tested positive for salmonella. The recall is classified as Class I and remains ongoing.
Which Products Are Affected
Organic Moringa Powder; 15kg/bag (bulk); Product code: GJ96. Lot: 25/08001. Expiration date: 02-11-2028. Total quantity: 2,490 kg. The product was distributed to 4 different consignees who used the ingredient for further processing and distribution.
What You Should Do
The recalling firm notified consignees via e-mail. No additional consumer instructions are provided in the recall notice.
Why This Matters
This is a Class I recall involving a food ingredient found positive for salmonella, distributed within the United States.
Source
FDA recall number H-1180-2026
Original source: FDA Official Notice ↗
Related FDA Recalls
All FDA Recalls →Nationwide notices with similar length or severity timing 8
Two Areazine-derived peer sets for this FDA recall: nearest notices by body length and by same severity near the same agency date. Peers come from other categories so they are not the same-feed Related list above.
Similar body length
Nearest notices by article body length (814 characters here).
Similar severity timing
Same severity (high) notices issued closest in time to August 11, 2026.
Frequently Asked Questions
Common questions about this FDA recall.