Beacon Promotions recalls repackaged M&M's in 20 states

FDA categorizes recall as Class II due to missing allergen information

Published on Feb. 7, 2026

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Beacon Promotions Inc. has initiated a voluntary recall of several repackaged M&M's products after the U.S. Food and Drug Administration (FDA) categorized the recall as Class II due to undeclared allergens including milk, soy, and peanut. The recalled products were distributed to 20 states across the country.

Why it matters

Food recalls due to undeclared allergens are serious, as they can pose a health risk to those with allergies to the missing ingredients. This recall highlights the importance of proper labeling and transparency from food manufacturers to ensure consumer safety.

The details

The recalled products include 1.3-ounce repackaged M&M's Peanut Candies labeled as 'Make Your Mark' and various 1.3-ounce repackaged M&M's Candies with promotional labels for different companies. The products were distributed to 20 states, including Alabama, Arizona, California, Florida, and others.

  • The recall was initiated by Beacon Promotions Inc. on January 26, 2026.
  • The FDA categorized the recall as Class II on February 4, 2026.

The players

Beacon Promotions Inc.

The company that initiated the voluntary recall of the repackaged M&M's products.

U.S. Food and Drug Administration (FDA)

The federal agency that categorized the recall as Class II due to the undeclared allergens.

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The takeaway

This recall underscores the importance of thorough allergen labeling and transparency from food manufacturers to ensure consumer safety, especially for those with food allergies. It serves as a reminder for shoppers to always check product labels carefully before consuming any food items.