RecallHawk
Class I Recall

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

Lund Food Holdings Inc

Summary

The FDA issued a Class I for Lunds & Byerlys Monster Cookies, Net Wt 10.0 oz (284g).. UPC 0 18169-66862 7. L by Lund Food Holdings Inc. Reason: Undeclared allergens (Peanut, Egg, Soy).

Details

Source

Food Recall

External ID

H-0352-2026

Action Date

2026-01-14

Status

Terminated

Category

food

Product Description

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

Lot/Code Info: Lot 501301

Quantity Affected: 108 cases (12 units per case)

Reason for Recall

Undeclared allergens (Peanut, Egg, Soy)

Distribution

MN

Type: Voluntary: Firm initiated

Recall Initiated: 2025-12-03

Company

Lund Food Holdings Inc

Eden Prairie, MN

Context & Analysis

This is a Class I recall. Class I recalls are the most serious — there is a reasonable probability that use of or exposure to the product will cause serious health consequences or death.

This was one of 36 food recalls issued in the same week, part of 204 food-related FDA actions this month.

Lund Food Holdings Inc has 2 FDA actions in our database, including 2 recalls.

Frequently Asked Questions

What is a Class I recall?

A Class I recall is the most serious type. The FDA has determined there is a reasonable probability that the product will cause serious adverse health consequences or death. Consumers should stop using the product immediately.

What should I do if I have this product?

Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (Lund Food Holdings Inc) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does Lund Food Holdings Inc have FDA actions?

Lund Food Holdings Inc has 2 FDA actions in our database, including 2 recalls and 0 device clearances.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "H-0352-2026" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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