Overview
- Keurig Dr Pepper initiated a voluntary recall on Dec. 6, 2025 after finding some McCafé Premium Roast Decaf K‑Cup pods may contain regular caffeinated coffee due to a labeling error.
- The FDA classified the action as a Class II recall on Jan. 23, indicating potential temporary or medically reversible adverse health effects with a remote chance of serious harm.
- The recall covers about 960 cartons, each with 84 pods (roughly 80,640 pods), distributed through a single retailer in California, Indiana and Nevada.
- Affected 84‑count cartons can be identified by UPC 043000073438, best‑by 17 NOV 2026, batch 5101564894, material number 5000358463 and ASIN B07GCNDL91.
- Consumers should stop using the pods and return or discard them; Keurig says buyers were notified in December and remaining retail stock was returned, no illnesses have been reported, and customer service is available at 866‑901‑2739.