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Lower risk Food recall · FDA · Published September 15, 2017

KIND Dark Chocolate Nuts Bar Recall: Missing Walnut Allergen Label

KIND LLC recalls 12-pack of Dark Chocolate Nuts and Sea Salt bars due to missing walnut allergen label on outer box. This poses a risk for people with walnut allergies. No action needed as the bars themselves are labeled.

🇺🇸 FDA recall #F-0001-2018FoodKIND ›
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Recalling firmKIND LLC1372 Broadway, 3rd FL · New York, NY 10018-6107
✎ GovInfoNow plain-language explainer

What happened, in plain English

KIND LLC is recalling 12-pack bars of Dark Chocolate Nuts and Sea Salt because the outer box doesn't list walnuts as an allergen. This could affect people with walnut allergies who might not know the product contains them. The bars themselves are properly labeled, so the risk is only for those with specific allergies. Read more at govinfonow.com/recall/20429-kind-dark-chocolate-nuts-bar-recall-missing-walnut-allergen-label.

Source Summary by GovInfoNow · govinfonow.com/recall/20429-kind-dark-chocolate-nuts-bar-recall-missing-walnut-allergen-label · Updated October 7, 2026 · FDA enforcement record: FDA #F-0001-2018

Cite this page

“KIND Dark Chocolate Nuts Bar Recall: Missing Walnut Allergen Label.” GovInfoNow, updated October 7, 2026. https://govinfonow.com/recall/20429-kind-dark-chocolate-nuts-bar-recall-missing-walnut-allergen-label. Based on FDA recall #F-0001-2018 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-0001-2018%22&limit=1).

Why it’s dangerous

The outer box fails to declare walnuts as an allergen, which could lead to allergic reactions in people sensitive to nuts. However, the individual bars are properly labeled with their ingredients, so the risk is limited to those with specific allergies.

Who’s affected

People with walnut allergies who consume the product may be at risk of allergic reactions. The recall affects KIND Dark Chocolate Nuts and Sea Salt bars sold in the U.S. from 2017 to 2018.

How to tell if you have this one

Check for the box with UPC 02652 17751 that contains 12 bars of Dark Chocolate Nuts and Sea Salt. The product was sold between December 2017 and February 2018 with best-by dates of 12/20/2017 or 2/3/2018.

  • Brand
    KIND
  • Product
    KIND Dark Chocolate Nuts and Sea Salt Bar-containing 12 /1.4 oz (40 g) bars Box :16.08 oz (480 g) per pack. Box UPC
  • Category
    Food
Based on the official FDA remedy

What to do — step by step

  1. Check Product Label

    Look for the box with UPC 02652 17751 that contains 12 bars of Dark Chocolate Nuts and Sea Salt.

Where it went and when

Where it was distributed

Distributed nationwide.

Alaska: yesAKMaine: yesMEVermont: yesVTNew Hampshire: yesNHWashington: yesWAIdaho: yesIDMontana: yesMTNorth Dakota: yesNDMinnesota: yesMNIllinois: yesILWisconsin: yesWIMichigan: yesMINew York: yesNYRhode Island: yesRIMassachusetts: yesMAOregon: yesORNevada: yesNVWyoming: yesWYSouth Dakota: yesSDIowa: yesIAIndiana: yesINOhio: yesOHPennsylvania: yesPANew Jersey: yesNJConnecticut: yesCTCalifornia: yesCAUtah: yesUTColorado: yesCONebraska: yesNEMissouri: yesMOKentucky: yesKYWest Virginia: yesWVVirginia: yesVAMaryland: yesMDDelaware: yesDEArizona: yesAZNew Mexico: yesNMKansas: yesKSArkansas: yesARTennessee: yesTNNorth Carolina: yesNCSouth Carolina: yesSCDistrict of Columbia: yesDCOklahoma: yesOKLouisiana: yesLAMississippi: yesMSAlabama: yesALGeorgia: yesGAHawaii: yesHITexas: yesTXFlorida: yesFL

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

Distributed nationwide.

Recall timeline

FDA terminated this recall 18 months after the firm started it.

1. Firm started the recall: Sep 15, 201712. FDA classified it Class II: Oct 3, 201723. Published in FDA’s Enforcement Report: Oct 11, 201734. FDA terminated the recall: Mar 8, 2019420172019
  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-0001-2018 (September 15, 2017) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-0001-2018 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