CLASS I Food recall · Reported 14 Jan 2026 · FDA Enforcement Report

Lunds & Byerlys Monster Cookies recalled by Lund Food Holdings

Lund Food Holdings is recalling Lunds & Byerlys Monster Cookies, distributed in Minnesota. The recall was initiated on 3 Dec 2025 and the FDA has classified it as Class I.

Check your package

Lot, batch or date codesLot 501301
Quantity recalled108 cases (12 units per case)

Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.

Recall details

Recall number
H-0352-2026
FDA event ID
98126
Recalling firm
Lund Food Holdings, Eden Prairie, MN
Brand
Lunds
Classification
Class I
Status
Terminated
Recall initiated
3 Dec 2025
FDA classified
5 Jan 2026
Reported
14 Jan 2026
Type
Voluntary: Firm initiated
Customers notified by
E-Mail
Reason category
Undeclared Allergens
Product category
Cookies

Timeline

3 Dec 2025Recall initiated by company
5 Jan 2026Classified by FDA+33 days
14 Jan 2026Published in enforcement report+9 days

Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.

Reason for recall

Undeclared allergens (Peanut, Egg, Soy)

Food allergen labelling is required by US law for the nine major allergens. A product recalled for an undeclared allergen is only a risk to people with that allergy; everyone else can consume it safely.

Product as listed by the FDA

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

Where it was distributed

MN

Minnesota

Questions about this recall

Why was it recalled?

Undeclared allergens (Peanut, Egg, Soy)

Which lots are affected?

Lot 501301

Where was it sold?

MN

What should I do if I have it?

Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.

What does Class I mean?

Class I is the most serious FDA recall category: there is a reasonable probability that using the product will cause serious health consequences or death.

Read the official FDA notice · Source record retrieved 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.

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