Repackaged M&Ms candies, Net Wt 1.3 oz. Item BB458BG. Labeled wit…

Beacon Promotions Inc has recalled Repackaged M&Ms candies, Net Wt 1.3 oz. Item BB458BG. Labeled wit…, according to data published by the U.S. Food and Drug Administration (FDA). The recall was reported on February 11, 2026 and was initiated on January 26, 2026. 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 Repackaged M&Ms candies, Net Wt 1.3 oz. Item BB458BG. Labeled wit…, with approximately 5788 units affected. The company behind the recall is Beacon Promotions Inc, based in Eagan, MN. The FDA describes the product as: “Repackaged M&Ms candies, Net Wt 1.3 oz. Item BB458BG. Labeled with the following promotional company names. 1. Next Up, 2. Smith Pro, 3. Jaxport, Jacksonville Port Authority, 4. Climax Molybdenum, A Freeport-McMoRan Company, 5. University of Maryland, School…”

Why was Repackaged M&Ms candies, Net Wt 1.3 oz. Item BB458BG. Labeled wit… recalled?

According to the FDA, the stated reason for the recall is: “Undeclared allergens (milk, soy, and peanut).” 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 Repackaged M&Ms candies, Net Wt 1.3 oz. Item BB458BG. Labeled wit…, compare it against the product description and identifying codes (Lot L450ARCLV03, Best By 12/1/2025 Lot L502FLHKP01, Best By 1/1/2026 Lot L523CMHKP01, Best By 6/30/2026 Lot L537GMHKP01, Best By 9/1/2026) before using it. This recall is currently listed as ongoing.

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 Beacon Promotions 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.