Class IITerminatedVoluntary: Firm initiated
Keurig DR Pepper, Inc.: food recall H-0419-2026
Keurig DR Pepper, Inc. of Knoxville, TN recalled McCafe Premium Roast Decaf Coffee K-Cup Pods, Net Wt. 29 oz (823g), packaged as an 84-count carton, UPC 043000073438.… Reason: Product is labeled as decaf, but might contain caffeine. The FDA listed it as Class II in its Enforcement Report dated Feb 4, 2026; distribution: California, Indiana, Nevada.
Record status as published: Terminated (terminated May 21, 2026). openFDA data last updated Oct 21, 2026.
Have this product? Check FDA.gov and your retailer. This page reproduces an FDA Enforcement Report record and is not a public alert. Look for the firm's recall notice on the FDA's recalls page, or ask the store where you bought it what to do. If you think you got sick from a food, contact a health care provider.
Recall details
- Product
- McCafe Premium Roast Decaf Coffee K-Cup Pods, Net Wt. 29 oz (823g), packaged as an 84-count carton, UPC 043000073438. Distributed By: Keurig Green Mountain, Inc. Burlington, MA 01803 U.S.A.
- Product quantity
- 960 cartons (84 pods/carton)
- Reason for recall
- Product is labeled as decaf, but might contain caffeine.
- Codes, lots and dates on the package
- Best By 17 NOV 2026 LA hh:mm PL070 5321 or 5322 Batch Number: 5101564894 Material Number: 5000358463 ASIN: B07GCNDL91
- Distribution pattern
- CA, IN, NV
- Recalling firm
- Keurig DR Pepper, Inc., Knoxville, TN
- Classification
- Class II — the FDA uses this class for a situation in which using or being exposed to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious adverse health consequences is remote.
- Voluntary or mandated
- Voluntary: Firm initiated
- How the firm first notified customers
- Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
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Dates
| Event | Date |
|---|---|
| Recall initiated by the firm | Dec 6, 2025 |
| Classified by the FDA | Jan 23, 2026 |
| Published in the Enforcement Report | Feb 4, 2026 |
| Terminated | May 21, 2026 |
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Sources
- U.S. Food and Drug Administration, openFDA food enforcement reports, recall number H-0419-2026 (openFDA record). Data provided by the U.S. Food and Drug Administration (https://open.fda.gov).
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