Enforcement WeeklyRegister of FDA actions · supplements, cosmetics, food
Records as of 2026-09-28 · 202 actions this year · not affiliated with the FDA

Class I · Recall · initiated July 8, 2026 · Ongoing

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Green Jeeva recalls bulk moringa powder already shipped to four manufacturers

A Cerritos, California ingredient supplier recalled 15 kg bags of organic moringa powder after the ingredient tested positive for Salmonella, after it had gone to four downstream firms for further processing.

The record

Firm
Green Jeeva LLC, Cerritos, CA
Product
Organic Moringa Powder; 15kg/bag (bulk); Product code: GJ96
Reason, as filed
“Moringa Powder ingredient positive for salmonella”
Classification
Class I (Class I: reasonable probability of serious health consequences or death)
Recall number
H-1180-2026
Initiated
July 8, 2026
Posted by FDA
July 29, 2026
Status
Ongoing · Voluntary: Firm initiated
Quantity
2,490 kg
Distribution
Product was distributed to 4 different consignees who have used the ingredient for further processing and distribution.

Verify: search any recall number above in FDA's enforcement report database.

Why it happened, in plain English

This is a supplier recall, not a brand recall. The product is a raw ingredient in 15 kg bulk bags, and the filed reason says the ingredient itself tested positive. The distribution line is the important part: four consignees had already used it “for further processing and distribution.” Whatever those four firms made from it is now exposed.

Moringa is a dried leaf. Drying does not kill Salmonella, it preserves it, and the organism survives in low-moisture powders for years. A bulk lot that tests positive was positive when it was packed. Nothing downstream, short of a validated kill step, changes that.

Who else should care

Any brand that buys botanical powders in bulk and encapsulates, blends or repacks them. Four firms bought this lot; FDA’s record does not name them. If you buy moringa or greens powder from a California distributor, ask which lots you received between spring and July 2026 and whether any came from this source.

The one thing to check: whether your incoming-ingredient acceptance relies on the supplier’s certificate of analysis alone. A COA describes the sample the supplier tested, not the bag you received.

Related actions

Written 2026-09-08. Analysis is editorial; the record above is FDA's.