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Lower risk Food recall · FDA · Published October 31, 2025

Bulk & Organic Moringa Powder Recall: Possible Salmonella Richmond Risk

Bulk & Organic LLC recalls 44.1lb bags of organic moringa powder due to possible Salmonella Richmond contamination. Consumers should check product codes and contact the company for details.

🇺🇸 FDA recall #H-0204-2026FoodBulk & Organic ›
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Contact the company

Recalling firmBULK & ORGANIC LLC206 Pegasus Ave · Northvale, NJ 07647-1909
✎ GovInfoNow plain-language explainer

Bulk & Organic LLC is recalling 44.1-pound bags of organic moringa powder after possible Salmonella Richmond contamination. This recall is important because Salmonella can cause foodborne illness, and affected products may be unsafe to eat. Read more at govinfonow.com/recall/7010-bulk-organic-moringa-powder-recall-possible-salmonella-richmond-risk.

Source Summary by GovInfoNow · govinfonow.com/recall/7010-bulk-organic-moringa-powder-recall-possible-salmonella-richmond-risk · Updated August 17, 2026 · Official notice: FDA #H-0204-2026

Cite this page

“Bulk & Organic Moringa Powder Recall: Possible Salmonella Richmond Risk.” GovInfoNow, updated August 17, 2026. https://govinfonow.com/recall/7010-bulk-organic-moringa-powder-recall-possible-salmonella-richmond-risk. Based on FDA recall #H-0204-2026.

BULK & ORGANIC LLC voluntarily recalled its Bulk and Organic Organic Moringa Powder, 44.1lbs bag due to possible Salmonella Richmond contamination, the FDA said on Oct. 31, 2025. The recall affects 565 bags distributed in New York, New Jersey, and California.

How to tell if you have it

  • Brand: Bulk & Organic
  • Product: Bulk and Organic Organic Moringa Powder, 44.1lbs bag
  • Code: VFD/ORG/MORP/L/24
  • Quantity: 565 bags
  • Distribution: NY, NJ, CA

The hazard

The product poses a risk of possible Salmonella Richmond contamination. The FDA classified the recall as Class I.

Context

GovInfoNow's records show other recent recalls of similar products include Green Jeeva Organic Moringa Powder Recall (2026-07-08), Food to Live Organic Moringa Leaf Powder Recalled Due to Salmonella Contamination (2025-11-11), and Trafa Organic Moringa Leaf Powder Recall (2026-06-24).

How to tell if you have this one

Check for the product code VFD/ORG/MORP/L/24 on the bag. The product is a 44.1-pound bag of organic moringa powder sold by Bulk & Organic LLC.

  • Brand
    Bulk & Organic
  • Category
    Food
Based on the official FDA remedy

What to do — step by step

  1. Check Product Code

    Look for the product code VFD/ORG/MORP/L/24 on the bag to confirm if it is recalled.

Where it went and when

Where it was distributed

Distributed in 3 states.

Alaska: not listedAKMaine: not listedMEVermont: not listedVTNew Hampshire: not listedNHWashington: not listedWAIdaho: not listedIDMontana: not listedMTNorth Dakota: not listedNDMinnesota: not listedMNIllinois: not listedILWisconsin: not listedWIMichigan: not listedMINew York: yesNYRhode Island: not listedRIMassachusetts: not listedMAOregon: not listedORNevada: not listedNVWyoming: not listedWYSouth Dakota: not listedSDIowa: not listedIAIndiana: not listedINOhio: not listedOHPennsylvania: not listedPANew Jersey: yesNJConnecticut: not listedCTCalifornia: yesCAUtah: not listedUTColorado: not listedCONebraska: not listedNEMissouri: not listedMOKentucky: not listedKYWest Virginia: not listedWVVirginia: not listedVAMaryland: not listedMDDelaware: not listedDEArizona: not listedAZNew Mexico: not listedNMKansas: not listedKSArkansas: not listedARTennessee: not listedTNNorth Carolina: not listedNCSouth Carolina: not listedSCDistrict of Columbia: not listedDCOklahoma: not listedOKLouisiana: not listedLAMississippi: not listedMSAlabama: not listedALGeorgia: not listedGAHawaii: not listedHITexas: not listedTXFlorida: not listedFL

FDA distribution: “NY, NJ, CA” States read from FDA’s own wording; “not listed” means the notice does not name it.

States: California, New Jersey, New York.

Recall timeline

FDA terminated this recall 9 months after the firm started it.

1. Firm started the recall: Oct 31, 202512. FDA classified it Class I: Nov 20, 202523. Published in FDA’s Enforcement Report: Nov 26, 202534. FDA terminated the recall: Jul 31, 2026420252026
  1. Firm started the recall
  2. FDA classified it Class I
  3. Published in FDA’s Enforcement Report
  4. FDA terminated the recall

Dates from the agency record only; steps without a date are left out.

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Where this comes from

The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.

  • Official source: FDA Recall #H-0204-2026 (October 31, 2025)
  • Plain-language summary written by qwen3:4b on August 17, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
  • GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.
GovInfoNow is an independent guide. We are not FDA or any government agency. Always confirm details with the official recall.Data: CPSC · FDA · NHTSA · USDA