Food recall

Lund Food Holdings Inc recall: Lunds & Byerlys Monster Cookies

Lund Food Holdings Inc, of Eden Prairie, MN, recalled Lunds & Byerlys Monster Cookies. The FDA's reason: “Undeclared allergens (Peanut, Egg, Soy).” The FDA classified it Class I: it could cause serious harm or death. The company began the recall voluntarily on December 3, 2025, and the FDA first listed it in its Enforcement Report of January 14, 2026. The FDA has closed the recall: it found the company did all it reasonably could to remove or correct the product.

How serious

Class I

It could cause serious harm or death

Why

Allergen not on the label

Status

Terminated

Closed April 8, 2026

The recall

Company
Lund Food Holdings Inc (Eden Prairie, MN)
Reason, in FDA's words
“Undeclared allergens (Peanut, Egg, Soy)”
Where it was sold
MN
Recall began
, by the company
FDA classified it
First in an FDA Enforcement Report
FDA event number
98126

The product recalled

As the FDA describes them, with the codes that tell whether a package is part of the recall.

  • H-0352-2026 Class I

    Lunds & Byerlys Monster Cookies, Net Wt 10.0 oz (284g).. UPC 0 18169-66862 7. Lunds & Byerlys, Edina, MN 55424

    Codes: Lot 501301

    Quantity: 108 cases (12 units per case)

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Source and notes

U.S. Food and Drug Administration, Enforcement Reports (openFDA food recall data) (Public domain (U.S. government work); source U.S. Food and Drug Administration, openFDA), data as of January 14, 2026.

Each week the FDA lists the recalls it has classified in its Enforcement Report, often weeks after the company announced the recall, so a month with five weekly reports tends to count more. Each recall counts once, however many products it covers, in the month FDA first listed it. Class I means the food could cause serious harm or death, Class II temporary or minor harm, and Class III is unlikely to harm anyone. Meat, poultry and most egg products are recalled by the U.S. Department of Agriculture, not the FDA, and aren't included. For what to do with a recalled product, see the FDA's recalls page.