FDA recall record

Beacon Promotions Repackaged M&Ms candies, Net Wt 1.3 oz recall — FDA H-0462-2026

Undeclared allergens (milk, soy, and peanut)

Class IIclassification
H-0462-2026official record ID
Feb 11, 2026report date

Recall record at a glance

Official recordH-0462-2026
CategoryFood Recalls
ClassificationClass II
FDA record statusOngoing
Recalling firmBeacon Promotions Inc
Report dateFeb 11, 2026
Recall initiation dateJan 26, 2026
Quantity5788 units
LocationEagan, MN, United States

Official product description

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 of Public Policy, 6. Liberty University Environmental Health & Safety, 7. Subaru, 8. Trinity Cyb3r, 9. Candy Treats, 10. JSE, Jordan & Skala Engineers, 11. Dropbox DocSend, 12. PP, Prosperity Promotions, 13. Northwest Indian College Foundation, 14. FES Branding Solutions, 15. Berkshire Hathaway Guard Insurance Companies, 16. merry maids Annual 26 Conference, 17. BW, Best Western, 18. Morgan Stanley, 19. tufin, 20. Compliments of Pioneer, 21. A.D. Morgan, Construction Manager, Design Builder, General Contractor, 22. Adobe, 23. xfinity, 24. Fundermax Interiors, 25. White Cup, 26. Acadia Commercial, 27. Aviagen, 28. ORG Expo, 29. Make Your Mark For nutrition facts, information, and ingredients, go to https://hpgbrands.com/sugarspot-nutrition/

Why the product was recalled

Undeclared allergens (milk, soy, and peanut)

Distribution information

AL, AZ, CA, FL, IA, KS, KY, MA, MD, MN, NC, NY, OH, PA, SD, TN, TX, VA, WA, WI

How to read the classification

FDA Class II indicates a situation in which use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote. The classification shown here comes from the FDA record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: E-Mail.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

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