CLASS II Food recall · Reported 29 Oct 2025 · FDA Enforcement Report

Lunds & Byerly's Premium confections recalled by Abdallah Incorporated

Abdallah Incorporated is recalling Lunds & Byerly's Premium confections, distributed in Minnesota. The recall was initiated on 30 Sep 2025 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codesLot Number: 079Y Best By Date: Jan 29, 2026
Quantity recalled744 units

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-0099-2026
FDA event ID
97727
Recalling firm
Abdallah Incorporated, Apple Valley, MN
Brand
Lunds
Classification
Class II
Status
Terminated
Recall initiated
30 Sep 2025
FDA classified
20 Oct 2025
Reported
29 Oct 2025
Type
Voluntary: Firm initiated
Customers notified by
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Reason category
Undeclared Tree Nuts
Product category
Candy

Timeline

30 Sep 2025Recall initiated by company
20 Oct 2025Classified by FDA+20 days
29 Oct 2025Published 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

Pecan Caramel Clusters may contain undeclared cashews.

Product as listed by the FDA

Lunds & Byerly's Premium confections. Pecan Caramel Cluster Dipped in milk chocolate. Net Wt 2.5 oz (71g) UPC 0 72431-01294 5. Produced for Lunds & Byerlys, Edina, MN 55424.

Where it was distributed

MN

Minnesota

Questions about this recall

Why was it recalled?

Pecan Caramel Clusters may contain undeclared cashews.

Which lots are affected?

Lot Number: 079Y Best By Date: Jan 29, 2026

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 II mean?

Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.

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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