CLASS I Food recall · Reported 26 Nov 2025 · FDA Enforcement Report

Organic Moringa Powder recalled by Bulk & Organic

Bulk & Organic is recalling Organic Moringa Powder, distributed in California, New Jersey, New York. The recall was initiated on 31 Oct 2025 and the FDA has classified it as Class I.

Check your package

Lot, batch or date codesVFD/ORG/MORP/L/24
Quantity recalled565 bags

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-0204-2026
FDA event ID
97925
Recalling firm
Bulk & Organic, Northvale, NJ
Brand
Bulk
Classification
Class I
Status
Terminated
Recall initiated
31 Oct 2025
FDA classified
20 Nov 2025
Reported
26 Nov 2025
Type
Voluntary: Firm initiated
Customers notified by
E-Mail
Reason category
Salmonella
Product category
Herbal Supplements

Timeline

31 Oct 2025Recall initiated by company
20 Nov 2025Classified by FDA+20 days
26 Nov 2025Published in enforcement report+6 days

Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.

Reason for recall

Possible Salmonella Richmond

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

Bulk and Organic Organic Moringa Powder, 44.1lbs bag

Where it was distributed

NY, NJ, CA

CaliforniaNew JerseyNew York

Questions about this recall

Why was it recalled?

Possible Salmonella Richmond

Which lots are affected?

VFD/ORG/MORP/L/24

Where was it sold?

NY, NJ, CA

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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