Keurig Recalls McCafé Premium Roast Decaf Coffee K-Cup Pods Due to Labeling Error
Keurig has announced a recall of over 80,000 of its K-Cup coffee pods due to a labeling error. The affected product is the McCafé Premium Roast Decaf Coffee K-Cup Pods, which are labeled as decaf but may still contain caffeine. The Food and Drug Administration has classified this recall as a Class II risk, indicating a potential health hazard if consumed. The affected pods were distributed in California, Indiana, and Nevada with a "best by" date of Nov. 17, 2026, and can be identified by specific batch and material numbers. Customers who have purchased these pods are advised to either dispose of them or return them for a refund or replacement.
It is important to note that the recall affects the McCafé Premium Roast Decaf Coffee K-Cup Pods from Keurig. These pods were mistakenly labeled as decaf but may contain caffeine, posing a potential health risk if consumed. The Food and Drug Administration has classified this recall as a Class II risk, indicating the severity of the issue. Customers who have purchased these pods in California, Indiana, and Nevada with a "best by" date of Nov. 17, 2026, are advised to check the batch and material numbers for identification and take appropriate action.
If you have purchased the McCafé Premium Roast Decaf Coffee K-Cup Pods from Keurig, be aware that a labeling error has led to a recall of over 80,000 pods. Despite being labeled as decaf, these pods may still contain caffeine, which could pose a health risk if consumed. The affected pods were distributed in California, Indiana, and Nevada with a "best by" date of Nov. 17, 2026, and can be identified by specific batch and material numbers. Customers who have purchased these pods are urged to either dispose of them or return them for a refund or replacement.
In summary, Keurig has issued a recall of its McCafé Premium Roast Decaf Coffee K-Cup Pods due to a labeling error that may result in the pods containing caffeine despite being labeled as decaf. The Food and Drug Administration has classified this recall as a Class II risk, indicating a potential health hazard. Customers who have purchased these pods in California, Indiana, and Nevada with a "best by" date of Nov. 17, 2026, should check the batch and material numbers for identification and take appropriate action, such as disposing of the pods or returning them for a refund or replacement.