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FDA Classifies Repackaged M&Ms Recall in 20 States as Class II

The action targets promotional packs missing required milk, soy, peanut disclosures, posing a risk only to allergic consumers.

Overview

  • Beacon Promotions initiated the voluntary recall on January 26 after discovering labeling errors on 1.3-ounce packs repackaged for clients.
  • FDA notices show more than 6,000 units are affected across two groups: 5,788 units (item BB458BG) and 541 units (item BB471BG) tied to specific lot codes with best-by dates through September 1, 2026.
  • The mislabeled candy was distributed under numerous corporate and event-branded promotional labels and shipped to 20 states.
  • As of February 4, regulators reported no illnesses linked to the recalled products, and the recall remains active.
  • People with milk, soy or peanut allergies are advised to discard or return the affected packs, while those without these allergies can safely consume them.