Zoe's Cookies Vegan Tuxedo Fudge Recall: Undeclared Walnuts in Cookies
Dough-To-Go Inc. recalls Zoe's Cookies Vegan Tuxedo Fudge due to undeclared walnuts. Consumers should check for the specific UPC 044964-13340 and lot 222620.
Lower-risk recall
Undeclared allergen; walnuts
Contact the company
What happened, in plain English
Dough-To-Go Inc. is recalling Zoe's Cookies Vegan Tuxedo Fudge cookies because they contain undeclared walnuts, a known allergen. This recall affects people with walnut allergies who may experience allergic reactions if they consume the product. Read more at govinfonow.com/recall/19096-zoe-s-cookies-vegan-tuxedo-fudge-recall-undeclared-walnuts-in.
Source Summary by GovInfoNow · govinfonow.com/recall/19096-zoe-s-cookies-vegan-tuxedo-fudge-recall-undeclared-walnuts-in · Updated October 7, 2026 · FDA enforcement record: FDA #F-1537-2018
Cite this page
“Zoe's Cookies Vegan Tuxedo Fudge Recall: Undeclared Walnuts in Cookies.” GovInfoNow, updated October 7, 2026. https://govinfonow.com/recall/19096-zoe-s-cookies-vegan-tuxedo-fudge-recall-undeclared-walnuts-in. Based on FDA recall #F-1537-2018 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-1537-2018%22&limit=1).
Why it’s dangerous
The cookies contain walnuts that were not listed in the ingredients, which can cause allergic reactions in individuals sensitive to nuts. The product was manufactured on shared equipment with tree nuts, increasing the risk of cross-contamination.
Who’s affected
People with walnut allergies are at risk of allergic reactions from consuming these cookies. The recall applies to specific lots produced by Dough-To-Go Inc.
How to tell if you have this one
Check for the UPC 044964-13340 and lot number 222620 on the packaging. The product is a 4 oz. individually wrapped cookie from Dough-To-Go Inc.
- Brand
Zoe's Cookies- Product
Zoe's Cookies Vegan Tuxedo Fudge, 4 oz. (153 kg) individually wrapped cookie. INGREDIENTS: UNBLEACHED FLOUR (WHEAT- Category
Food
What to do — step by step
Check Product Label
Look for the UPC 044964-13340 and lot number 222620 on the packaging.
Where it went and when
Where it was distributed
Distributed in California.
FDA distribution: “U.S. distribution to the following: CA. No foreign distribution.” States read from FDA’s own wording; “not listed” means the notice does not name it.
States: California.
Recall timeline
FDA terminated this recall 3 months after the firm started it.
- Firm started the recall
- FDA classified it Class I
- Published in FDA’s Enforcement Report
- 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-1537-2018 (May 24, 2018) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-1537-2018 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.