Dark Chocolate Coffee Beans (JLM Manufacturing) – Undeclared Ingredients (2017)
Class II: A situation in which use of, or exposure to, a violative product may cause temporary or medically reversible adverse health consequences or where the probability of serious adverse health consequences is remote
Class II recall indicates potential for temporary health effects.
This AI-generated summary is provided for general informational purposes only and is derived from publicly available recall notices. It supplements but does not replace official agency classifications or safety instructions.
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Dark Chocolate Coffee Beans, Natural Dark Chocolate Coffee Beans
Brand
JLM Manufacturing LLC
Lot Codes / Batch Numbers
ALL NATURAL, NATURAL COFFEE BEANS DARK CHOCOLATE, Product Number: 452760, Pack/Size 12/8 oz., Best BY Date: February 2017 October UPC: 2018 94776128235 JLM TUB, TUB LG COFFEE BEANS DARK CHOCOLATE, Product Number: 477308, Pack/Size: 12/12 oz, Best By Date:. February 2017 October 2018, UPC: 94776131761
Products Sold
ALL NATURAL, NATURAL COFFEE BEANS DARK CHOCOLATE, Product Number: 452760, Pack/Size 12/8 oz., Best BY Date: February 2017 October UPC: 2018 94776128235 JLM TUB, TUB LG COFFEE BEANS DARK CHOCOLATE, Product Number: 477308, Pack/Size: 12/12 oz, Best By Date:. February 2017 October 2018, UPC: 94776131761
JLM Manufacturing LLC is recalling Dark Chocolate Coffee Beans, Natural Dark Chocolate Coffee Beans due to JLM Manufacturing LLC is recalling multiple dark chocolate products due to a supplier's recall for undeclared ingredient butterfat, and undeclared all. This is a Class I recall, indicating a high risk of serious health consequences. Based on FDA enforcement report.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
JLM Manufacturing LLC is recalling multiple dark chocolate products due to a supplier's recall for undeclared ingredient butterfat, and undeclared allergen milk.
Recommended Action
Per FDA guidance
Consumers should stop using the product and contact the recalling firm or return it to the place of purchase.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticeDistribution
As reported by FDA
AL, FL, IL, IN, IA, KY, LA, MI, MN, MO, NE, OH, PA, SC, TN, VA, WV, WI
Page updated: Jan 6, 2026