RecallRadar
High RiskReported January 14, 2026

Lunds & Byerlys Monster Cookies

Recalled by Lund Food Holdings Inc

Food recall

Lund Food Holdings Inc

Class I — most serious

There is a reasonable chance that using this product could cause serious health problems or death.

See all recalls involving an undeclared allergen

Lund Food Holdings Inc has recalled Lunds & Byerlys Monster Cookies, according to data published by the U.S. Food and Drug Administration (FDA). The recall was reported on January 14, 2026 and was initiated on December 3, 2025. It is classified as a Class I recall, which means there is a reasonable chance that using this product could cause serious health problems or death.

Below is a plain-English summary of what was recalled, why it was recalled, how to tell whether you have the affected product, and what steps you can take. For the complete and most current details, you can view the FDA record linked further down this page.

What was recalled?

This recall covers Lunds & Byerlys Monster Cookies, with approximately 108 cases (12 units per case) affected. The company behind the recall is Lund Food Holdings Inc, based in Eden Prairie, MN. The FDA describes the product as: “Lunds & Byerlys Monster Cookies, Net Wt 10.0 oz (284g).. UPC 0 18169-66862 7. Lunds & Byerlys, Edina, MN 55424”

Why was Lunds & Byerlys Monster Cookies recalled?

According to the FDA, the stated reason for the recall is: “Undeclared allergens (Peanut, Egg, Soy).” In plain terms, this recall relates to an undeclared ingredient or allergen.

An undeclared ingredient means a food contains something — often a major allergen such as milk, eggs, soy, wheat, peanuts, or tree nuts — that is not listed on the label. For most people this is not dangerous, but for someone with a food allergy or sensitivity it can trigger a serious reaction. Accurate labeling is required so that people can avoid ingredients they need to stay away from.

What should you do?

If you think you may have bought Lunds & Byerlys Monster Cookies, compare it against the product description and identifying codes (Lot 501301) before using it.

The general guidance for a matching product is to stop using it and follow the instructions in the official FDA recall notice, which may include a repair, replacement, refund, or safe disposal. When in doubt, contact Lund Food Holdings Inc or your local health authority.

About this recall

This recall was distributed in MN. RecallRadar summarizes recall information from public FDA data to make it easier to understand. We are an independent service and are not affiliated with the FDA or any government agency, so please always refer to the official source for the authoritative record — and note the “last synced” date shown on this page, since recall details can change over time.

Full recall details

Status
Terminated
Date reported
January 14, 2026
Recall started
December 3, 2025
Distributed in
MN
What was recalled
Lunds & Byerlys Monster Cookies, Net Wt 10.0 oz (284g).. UPC 0 18169-66862 7. Lunds & Byerlys, Edina, MN 55424
Why it was recalled (as stated by the FDA)
Undeclared allergens (Peanut, Egg, Soy)
How to identify the affected product
Lot 501301
Amount recalled
108 cases (12 units per case)

What you can do

Check whether any product you have matches the description and codes above. If it does, stop using it and follow the instructions in the official recall notice. When in doubt, contact the company or your local health authority.

Quick answers

Why was Lunds & Byerlys Monster Cookies recalled?+

According to the FDA: Undeclared allergens (Peanut, Egg, Soy)

How serious is this recall?+

Class I — most serious. There is a reasonable chance that using this product could cause serious health problems or death.

What should I do if I have Lunds & Byerlys Monster Cookies?+

Compare your product against the description and identifying codes on this page. If it matches, stop using it and follow the instructions in the official recall notice — this usually means returning it for a refund or discarding it. When in doubt, contact the company or your local health authority.

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View the official FDA record

Opens the U.S. Food and Drug Administration (FDA) data for this recall.

Recall number: H-0352-2026. Information last synced from the FDA on July 5, 2026.