Lunds & Byerlys recalls 10oz Monster Cookies due to undeclared peanut, egg, and soy allergens. Consumers should check UPC 018169668627 for affected lots.
“Lunds & Byerlys Monster Cookies Recall: Undeclared Peanuts, Eggs, Soy Allergens.” GovInfoNow, updated August 18, 2026. https://govinfonow.com/recall/6922-lunds-byerlys-monster-cookies-recall-undeclared-peanuts-eggs-soy-allergens. Based on FDA recall #H-0352-2026.
Lund Food Holdings Inc. recalled Lunds & Byerlys Monster Cookies due to undeclared peanut, egg, and soy allergens, the FDA said on Dec. 3, 2025. The voluntary Class I recall affects products distributed in Minnesota.
The cookies contain undeclared peanut, egg, and soy allergens, posing a risk to consumers with allergies to these ingredients. The FDA classified the recall as Class I.
Context
GovInfoNow's records show Lund Food Holdings Inc. has one other recall on record since Sept. 27, 2024: the Lunds & Byerlys Lone Star Dip Recall for potential mold contamination on that date. Other recent recalls of similar products include Best Friends Bakery Recalls Pumpkin Spice Cookies for Peanut Allergy Risk (Aug. 17, 2026), Troemner Farm Pfeffernusse Cookies Recall: Undeclared Soy, Wheat, Milk (Dec. 19, 2025), and Nuts.com Espresso Malted Milk Balls Recall: Undeclared Wheat and Soy Allergens (March 10, 2026).
How to tell if you have this one
Check for the UPC 018169668627 on the packaging. The product was sold with lot number 501301.
Brand
Lunds & Byerlys
Product
Lunds & Byerlys Monster Cookies, Net Wt 10.0 oz (284g).. UPC 0 18169-66862 7. Lunds & Byerlys, Edina, MN 55424
Category
Food
Based on the official FDA remedy
What to do — step by step
Check Product Label
Look for the UPC 018169668627 and lot number 501301 on the package.
Where it went and when
Where it was distributed
Distributed in Minnesota.
Listed by the agency
Not listed
FDA distribution: “MN” States read from FDA’s own wording; “not listed” means the notice does not name it.
States: Minnesota.
Recall timeline
FDA terminated this recall 4 months after the firm started it.
1Firm started the recall
2FDA classified it Class I
3Published in FDA’s Enforcement Report
4FDA terminated the recall
Dates from the agency record only; steps without a date are left out.
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 #H-0352-2026 (December 3, 2025)
Plain-language summary written by qwen3:4b on August 18, 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.