The U.S. Food and Drug Administration has announced a recall involving repackaged M&M’s distributed as promotional giveaway items, citing missing allergen disclosures.
The recall does not affect standard retail M&M’s sold in stores.
According to the FDA, Beacon Promotions Inc. repackaged bulk M&M’s into 1.3‑ounce branded promotional bags for corporate and event distribution. The packages did not include required allergen statements for milk, soy, and peanuts, prompting a Class II recall. This classification indicates that exposure to the product could cause temporary or medically reversible health effects for individuals with allergies.
The recalled items were distributed under various promotional labels, including corporate and event branding such as “Make Your Mark,” Subaru, Adobe, and Morgan Stanley. Two product codes are included in the recall: BB458BG and BB471BG, covering several lot codes with best‑by dates ranging from December 2025 through September 2026.
The products were shipped to recipients in 20 states, including North Carolina. Because these items were distributed as giveaways rather than sold in stores, consumers may have received them at conferences, trade shows, corporate events, or through promotional mailings.
The recall applies only to the repackaged promotional bags. Mars‑manufactured retail M&M’s are not part of this recall.
Consumers who received the promotional items are advised not to eat them and to discard the product. Individuals with questions may contact Beacon Promotions or consult the FDA’s recall database for additional information.
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