FDA recall H-0419-2026 · Feb 4, 2026
Keurig DR Pepper, Inc.: McCafe Premium Roast Decaf Coffee K-Cup Pods recall
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.
Reason for recall
Product is labeled as decaf, but might contain caffeine.
What to do
FDA enforcement reports don't include consumer instructions. Check the codes below against your package, and look for the company's notice on FDA's recalls page. If you have the product and aren't sure, don't use it until you've checked.
Recall details
- FDA classification
- Class II: use of or exposure to the product may cause temporary or medically reversible health problems, or the chance of serious problems is remote.
- Status
- Terminated
- Codes, lots and dates
- Best By 17 NOV 2026 LA hh:mm PL070 5321 or 5322 Batch Number: 5101564894 Material Number: 5000358463 ASIN: B07GCNDL91
- Quantity
- 960 cartons (84 pods/carton)
- Distribution
- CA, IN, NV
- Recalling firm
- Keurig DR Pepper, Inc., Knoxville, TN
- Voluntary or mandated
- Voluntary: Firm initiated
- Recall started
- 2025-12-06
Source: openFDA enforcement record H-0419-2026 · search recall number H-0419-2026 in FDA's Enforcement Report.
Copied from the agency record without changes. Data as of Oct 14, 2026, 1:15 AM EDT. The agency notice is the final word.
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