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Lower risk Food recall · FDA · Published September 12, 2017

Natural Grocers Organic Deglet Dates Recall: Undeclared Coconut Hazard

Natural Grocers recalls organic deglet noor dates due to potential undeclared coconut. Consumers should check labels for lot code 198-17.

🇺🇸 FDA recall #F-3608-2017FoodNatural Grocers ›
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Recalling firmVitamin Cottage Natural Food Markets, Inc.12612 W Alameda Pkwy · Lakewood, CO 80228-2824
✎ GovInfoNow plain-language explainer

What happened, in plain English

Natural Grocers is recalling organic deglet noor dates that may contain undeclared coconut. This could pose a risk for people with coconut allergies. The recall affects specific packages sold at Target. Read more at govinfonow.com/recall/20434-natural-grocers-organic-deglet-dates-recall-undeclared-coconut-hazard.

Source Summary by GovInfoNow · govinfonow.com/recall/20434-natural-grocers-organic-deglet-dates-recall-undeclared-coconut-hazard · Updated October 7, 2026 · FDA enforcement record: FDA #F-3608-2017

Cite this page

“Natural Grocers Organic Deglet Dates Recall: Undeclared Coconut Hazard.” GovInfoNow, updated October 7, 2026. https://govinfonow.com/recall/20434-natural-grocers-organic-deglet-dates-recall-undeclared-coconut-hazard. Based on FDA recall #F-3608-2017 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-3608-2017%22&limit=1).

Why it’s dangerous

The dates may contain undeclared coconut, which can cause allergic reactions in sensitive individuals. This is a potential allergen issue rather than a physical hazard like choking or fire.

Who’s affected

People with coconut allergies are most at risk from this recall. The recall applies to Natural Grocers organic deglet noor dates sold at Target stores.

How to tell if you have this one

Check for the lot code 198-17 on the front label beneath the Net Weight. The product is sold in zip lock plastic bags with a target weight of 0.60 to 0.70 pounds.

  • Brand
    Natural Grocers
  • Category
    Food
Based on the official FDA remedy

What to do — step by step

  1. Check Label for Lot Code

    Look for lot code 198-17 on the front label beneath the Net Weight.

Where it went and when

Where it was distributed

Distributed in 11 states.

Alaska: not listedAKMaine: not listedMEVermont: not listedVTNew Hampshire: not listedNHWashington: yesWAIdaho: yesIDMontana: yesMTNorth Dakota: not listedNDMinnesota: not listedMNIllinois: not listedILWisconsin: not listedWIMichigan: not listedMINew York: not listedNYRhode Island: not listedRIMassachusetts: not listedMAOregon: yesORNevada: not listedNVWyoming: yesWYSouth Dakota: not listedSDIowa: not listedIAIndiana: not listedINOhio: not listedOHPennsylvania: not listedPANew Jersey: not listedNJConnecticut: not listedCTCalifornia: not listedCAUtah: yesUTColorado: yesCONebraska: not listedNEMissouri: yesMOKentucky: not listedKYWest Virginia: not listedWVVirginia: not listedVAMaryland: not listedMDDelaware: not listedDEArizona: yesAZNew Mexico: yesNMKansas: 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: yesTXFlorida: not listedFL

FDA distribution: “45 retail locations in Washington, Oregon, Idaho, Montana, Wyoming, Utah, Colorado, Arizona, New Mexico, Texas, Missouri . No foreign/VA/Govt/Military consignees.” States read from FDA’s own wording; “not listed” means the notice does not name it.

States: Arizona, Colorado, Idaho, Missouri, Montana, New Mexico, Oregon, Texas, Utah, Washington, Wyoming.

Recall timeline

FDA terminated this recall 5 months after the firm started it.

1. Firm started the recall: Sep 12, 201712. FDA classified it Class II: Sep 29, 201723. Published in FDA’s Enforcement Report: Oct 11, 201734. FDA terminated the recall: Feb 9, 2018420172018
  1. Firm started the recall
  2. FDA classified it Class II
  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-3608-2017 (September 12, 2017) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-3608-2017 to see it in context.
  • Plain-language summary written by qwen3:4b on October 7, 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