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Lower risk Food recall · FDA · Published October 26, 2016

DFI Organics Sesame Seeds Recall: Salmonella Risk in Uganda-Sourced Product

DFI Organics recalls 50-lb natural sesame seeds from Uganda due to potential Salmonella contamination. Consumers should check lot numbers LTI000292-1 and LTI0:000292-2 for affected products.

🇺🇸 FDA recall #F-0570-2017FoodDFI Organics ›
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Recalling firmDFI Organics575 Lexington Ave FL 4 · New York, NY 10022-6146
✎ GovInfoNow plain-language explainer

What happened, in plain English

DFI Organics is recalling 50-pound natural sesame seeds from Uganda that may contain Salmonella. This poses a risk of foodborne illness if consumed. Read more at govinfonow.com/recall/22975-dfi-organics-sesame-seeds-recall-salmonella-risk-in-uganda-sourced.

Source Summary by GovInfoNow · govinfonow.com/recall/22975-dfi-organics-sesame-seeds-recall-salmonella-risk-in-uganda-sourced · Updated October 9, 2026 · FDA enforcement record: FDA #F-0570-2017

Cite this page

“DFI Organics Sesame Seeds Recall: Salmonella Risk in Uganda-Sourced Product.” GovInfoNow, updated October 9, 2026. https://govinfonow.com/recall/22975-dfi-organics-sesame-seeds-recall-salmonella-risk-in-uganda-sourced. Based on FDA recall #F-0570-2017 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-0570-2017%22&limit=1).

Why it’s dangerous

Salmonella is a bacteria that can cause food poisoning. If the seeds contain Salmonella, eating them may lead to symptoms like diarrhea, fever, and abdominal cramps.

Who’s affected

Anyone who purchased DFI Organics' 50-lb natural sesame seeds from Uganda. People with weakened immune systems are at higher risk of foodborne illness.

How to tell if you have this one

Check for lot numbers LTI000292-1 and LTI000292-2 on the multi-ply paper bags. The product is 50 pounds of natural sesame seeds from Uganda.

  • Brand
    DFI Organics
  • Category
    Food
Based on the official FDA remedy

What to do — step by step

  1. Check Product Lot Number

    Look for lot numbers LTI000292-1 or LTI000292-2 on the multi-ply paper bags.

Where it went and when

Where it was distributed

Distributed in New Jersey.

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: not listedNYRhode 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: not listedCAUtah: 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: “New Jersey” States read from FDA’s own wording; “not listed” means the notice does not name it.

States: New Jersey.

Recall timeline

FDA terminated this recall 20 months after the firm started it.

1. Firm started the recall: Oct 26, 201612. FDA classified it Class I: Dec 6, 201623. Published in FDA’s Enforcement Report: Dec 14, 201634. FDA terminated the recall: Jun 19, 2018420162018
  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 #F-0570-2017 (October 26, 2016) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-0570-2017 to see it in context.
  • Plain-language summary written by qwen3:4b on October 9, 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