Food recall

Keurig DR Pepper, Inc. recall: McCafe Premium Roast Decaf Coffee K-Cup Pods

Keurig DR Pepper, Inc., of Knoxville, TN, recalled McCafe Premium Roast Decaf Coffee K-Cup Pods. The FDA's reason: “Product is labeled as decaf, but might contain caffeine.” The FDA classified it Class II: it could cause temporary or minor harm. The company began the recall voluntarily on December 6, 2025, and the FDA first listed it in its Enforcement Report of February 4, 2026. The FDA has closed the recall: it found the company did all it reasonably could to remove or correct the product.

How serious

Class II

It could cause temporary or minor harm

Why

Labeling, packaging or manufacturing problems

Status

Terminated

Closed May 21, 2026

The recall

Company
Keurig DR Pepper, Inc. (Knoxville, TN)
Reason, in FDA's words
“Product is labeled as decaf, but might contain caffeine.”
Where it was sold
CA, IN, NV
Recall began
, by the company
FDA classified it
First in an FDA Enforcement Report
FDA event number
98138

The product recalled

As the FDA describes them, with the codes that tell whether a package is part of the recall.

  • H-0419-2026 Class II

    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.

    Codes: 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)

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Source and notes

U.S. Food and Drug Administration, Enforcement Reports (openFDA food recall data) (Public domain (U.S. government work); source U.S. Food and Drug Administration, openFDA), data as of February 4, 2026.

Each week the FDA lists the recalls it has classified in its Enforcement Report, often weeks after the company announced the recall, so a month with five weekly reports tends to count more. Each recall counts once, however many products it covers, in the month FDA first listed it. Class I means the food could cause serious harm or death, Class II temporary or minor harm, and Class III is unlikely to harm anyone. Meat, poultry and most egg products are recalled by the U.S. Department of Agriculture, not the FDA, and aren't included. For what to do with a recalled product, see the FDA's recalls page.