Keurig has issued a voluntary recall of one of its popular K-Cup varieties.

The brand, known for its coffee makers and drink pods, shared details about the ongoing recall in a notice that was posted to the U.S. Food and Drug Administration (FDA) website.

Here’s everything you need to know.

Which Product Is Being Recalled and Why?

If you have McCafe Premium Roast Decaf Coffee K-Cup Pods at home, you may want to think twice before popping one into your Keurig machine.

In a recall notice, Keurig DR Pepper, Inc. noted that the product is “labeled as decaf, but might contain caffeine.”

The recall was first initiated on Dec. 6, 2025 and classified as a Class II recall on Jan. 23. The FDA’s Class II category typically means that a particular product “may cause temporary or medically reversible adverse health consequences or where the probability of serious adverse health consequences is remote.”

How to Tell If You Have the Product

Keurig has recalled 960 cartons of 29-ounce McCafe Premium Roast Decaf Coffee K-Cup Pods. Each carton contains 84 pods.

The recalled K-Cup pods have the following identifying details:

  • Recall number: H-0419-2026
  • Best by date: 17 NOV 2026
  • Batch Number: 5101564894
  • Material Number: 5000358463
  • ASIN: B07GCNDL91
  • UPC 043000073438

The recalled K-Cup pods were distributed in California, Indiana and Nevada.

What to Do If You Have the Product

Consumers were notified directly by retailers about how to replace their purchases and all affected products have been removed from store shelves, Keurig Dr Pepper told TODAY.com in a statement.