Lunds & Byerly's Premium confections. Pecan Caramel Cluster Dipped…

Abdallah Incorporated has recalled Lunds & Byerly's Premium confections. Pecan Caramel Cluster Dipped…, according to data published by the U.S. Food and Drug Administration (FDA). The recall was reported on October 29, 2025 and was initiated on September 30, 2025. It is classified as a Class II recall, which means using this product might cause a temporary or medically reversible health problem. The chance of serious harm is low.

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 & Byerly's Premium confections. Pecan Caramel Cluster Dipped…, with approximately 744 units affected. The company behind the recall is Abdallah Incorporated, based in Apple Valley, MN. The FDA describes the product as: “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.”

Why was Lunds & Byerly's Premium confections. Pecan Caramel Cluster Dipped… recalled?

According to the FDA, the stated reason for the recall is: “Pecan Caramel Clusters may contain undeclared cashews.” 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 & Byerly's Premium confections. Pecan Caramel Cluster Dipped…, compare it against the product description and identifying codes (Lot Number: 079Y Best By Date: Jan 29, 2026) 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 Abdallah Incorporated 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.