Overview
- The voluntary action, initiated Dec. 6, 2025, was classified by the FDA on Jan. 23 as a Class II recall.
- About 960 84-count cartons—roughly 80,640 pods—were sold through a single retailer to stores in California, Indiana and Nevada.
- Affected boxes carry a best-by date of 17 NOV 2026 and identifiers including batch 5101564894 and UPC 043000073438.
- Keurig Dr Pepper says customers were contacted by the retailer for replacements and all remaining stock was returned; no illnesses have been reported.
- Consumers are advised to stop using the pods and discard or return them for a refund or replacement, or call Keurig Consumer Care at 866-901-2739.