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Lower risk Food recall · FDA · Published August 1, 2017

Fairway Cookies Blondie Recall: Undeclared Walnuts in Product

Fairway recalls 10 oz. Cookies Blondie with undeclared walnuts. Consumers should check item codes 268492 or 263413 for affected products.

🇺🇸 FDA recall #F-3442-2017FoodFairway ›
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Recalling firmFairway Group Holdings Corp2284 12th Ave · New York, NY 10027-2316
✎ GovInfoNow plain-language explainer

What happened, in plain English

Fairway is recalling 10-ounce Cookies Blondie cookies that contain undeclared walnuts. This poses a risk for people with nut allergies who may react to the hidden walnuts. Read more at govinfonow.com/recall/20621-fairway-cookies-blondie-recall-undeclared-walnuts-in-product.

Source Summary by GovInfoNow · govinfonow.com/recall/20621-fairway-cookies-blondie-recall-undeclared-walnuts-in-product · Updated October 7, 2026 · FDA enforcement record: FDA #F-3442-2017

Cite this page

“Fairway Cookies Blondie Recall: Undeclared Walnuts in Product.” GovInfoNow, updated October 7, 2026. https://govinfonow.com/recall/20621-fairway-cookies-blondie-recall-undeclared-walnuts-in-product. Based on FDA recall #F-3442-2017 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-3442-2017%22&limit=1).

Why it’s dangerous

The cookies contain walnuts that are not listed on the label, which can cause allergic reactions in people sensitive to nuts. This is a food safety issue for those with nut allergies who may not have been aware of the walnuts in the product.

Who’s affected

People with nut allergies are at risk from these cookies, as they contain undeclared walnuts. The recall affects Fairway Cookies Blondie products sold with item codes 268492 or 263413.

How to tell if you have this one

Check for Fairway Cookies Blondie 10 oz. products with item codes 268492 or 263413. All products have a 'SELL BY' date code.

  • Brand
    Fairway
  • Category
    Food
Based on the official FDA remedy

What to do — step by step

  1. Check Product Label

    Look for item codes 268492 or 263413 on the packaging to confirm if the product is affected.

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: yesCTCalifornia: 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 York, New Jersey and Connecticut” States read from FDA’s own wording; “not listed” means the notice does not name it.

States: Connecticut, New Jersey, New York.

Recall timeline

FDA terminated this recall 22 days after the firm started it.

1. Firm started the recall: Aug 1, 201712. FDA classified it Class II: Aug 22, 201723. FDA terminated the recall: Aug 23, 201734. Published in FDA’s Enforcement Report: Aug 30, 201742017
  1. Firm started the recall
  2. FDA classified it Class II
  3. FDA terminated the recall
  4. Published in FDA’s Enforcement Report

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-3442-2017 (August 1, 2017) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-3442-2017 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