Over 80,000 Keurig decaf pods recalled for possibly containing caffeinated coffee
Keurig Dr Pepper recalled 80,640 McCafé decaf pods due to a labeling error, with the FDA classifying it a Class II recall indicating possible temporary health effects.
- On December 6, Keurig Dr Pepper voluntarily recalled more than 80,000 McCafé Premium Roast Decaf Coffee K-Cup Pods after the FDA found they may contain caffeine.
- Health guidance warns that people limiting caffeine for health conditions, pregnancy or sensitivity should not consume the recalled K-Cup pods, as unexpected caffeine may cause jitters or sleep disruption.
- Newsweek contacted Keurig Dr Pepper via email outside regular business hours on Tuesday and reported from Washington, D.C. using information from an FDA recall letter.
66 Articles
66 Articles
FDA Announces Recall of More Than 80,000 Keurig Coffee Pods Sold in 3 States
The recalled coffee pods were sold exclusively on Amazon, said Keurig Dr Pepper. Ekaterina Sidorova / Getty Images / Health.comMore than 80,600 Keurig coffee pods were recalled in three states.The McCafé Decaf K-Cups may actually contain caffeine.The FDA gave the recall the second-highest risk level, Class II.More than 80,600 Keurig coffee pods have been recalled in three states, according to the Food and Drug Administration (FDA). McCafé Decaf …
More than 80,000 popular Keurig coffee pods recalled: What to know
Feeling jittery? More than 80,000 Keurig coffee pods labeled decaf have been recalled because they may in fact contain caffeine, an FDA enforcement report said. According to the report Keurig Inc., which makes popular coffee pods known as K-Cups, issued the recall Dec. 6, 2025. On Jan. 23, 2026, the FDA updated the enforcement report to classify the recall as “Class II.” The FDA says a Class II recall, which ranks as level two of three, applies …
Coverage Details
Bias Distribution
- 74% of the sources are Center
Factuality
To view factuality data please Upgrade to Premium























