FDA Recalls More Than 80,000 McDonald’s Coffee K-Cups Sold in Nevada

More than 80,000 McDonald’s-branded coffee K-Cup pods have been recalled after federal regulators determined the product may be mislabeled, according to the U.S. Food and Drug Administration.

The recall involves McCafé Premium Roast Decaf Coffee K-Cup pods that may contain caffeine despite being labeled as decaffeinated. The FDA classified the recall as a Class II recall, meaning use of the product could cause temporary or medically reversible health effects, particularly for individuals sensitive to caffeine.

The affected products were distributed to retailers in Nevada, California, and Indiana. The recalled coffee pods were sold in 84-count cartons and can be identified by a best-by date of November 17, 2026, and a specific batch number listed in the FDA notice.

Keurig Dr Pepper, which distributes the McDonald’s coffee pods, said the recall was issued voluntarily after the labeling issue was identified. The company stated that the affected products have been removed from store shelves and that consumers who purchased the recalled pods were notified by retailers.

Health officials advise consumers who have the recalled product not to use it and to follow return or refund instructions provided by the retailer. While caffeine exposure may not pose a risk for all consumers, it can be a concern for people with certain medical conditions or those avoiding caffeine for health reasons.

Source: 8 News Now, U.S. Food and Drug Administration.