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The FDA has issued a Class II recall for over 80,000 McCafe coffee pods labeled as decaf that may contain caffeine. Sold in three states, they pose health risks.
BURLINGTON, Mass. — The U.S. Food and Drug Administration on Tuesday elevated a voluntary recall of more than 80,000 coffee pods for incorrect labeling.
The coffee pods, sold by Keurig, are McCafe-branded and are labeled as decaf, but the FDA warned the pods may actually contain caffeine.
The recall was labeled as Class II, which means the products could cause temporary of medically reversible adverse health consequences. It’s the agency’s second-highest alert classification.
The pods were cold in nearly 1,000 84‑count cartons in California, Indiana, and Nevada, according to the recall. The affected cartons had a best-by date of Nov. 17, 2026, and had a batch number of 5101564894.
This is a developing situation. This article will be updated when more information is released.
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