RecallRadar
ModerateReported February 4, 2026

McCafe Premium Roast Decaf Coffee K-Cup Pods, Net Wt. 29 oz (823g)

Recalled by Keurig DR Pepper, Inc.

Food recall

Keurig DR Pepper, Inc.

Class II — moderate

Using this product might cause a temporary or medically reversible health problem. The chance of serious harm is low.

Keurig DR Pepper, Inc. has recalled McCafe Premium Roast Decaf Coffee K-Cup Pods, Net Wt. 29 oz (823g), according to data published by the U.S. Food and Drug Administration (FDA). The recall was reported on February 4, 2026 and was initiated on December 6, 2025. It is classified as a Class II recall, which means using this product might cause a temporary or medically reversible health problem. The chance of serious harm is low.

Below is a plain-English summary of what was recalled, why it was recalled, how to tell whether you have the affected product, and what steps you can take. For the complete and most current details, you can view the FDA record linked further down this page.

What was recalled?

This recall covers McCafe Premium Roast Decaf Coffee K-Cup Pods, Net Wt. 29 oz (823g), with approximately 960 cartons (84 pods/carton) affected. The company behind the recall is Keurig DR Pepper, Inc., based in Knoxville, TN. The FDA describes the product as: “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.”

Why was McCafe Premium Roast Decaf Coffee K-Cup Pods, Net Wt. 29 oz (823g) recalled?

According to the FDA, the stated reason for the recall is: “Product is labeled as decaf, but might contain caffeine.”

What should you do?

If you think you may have bought McCafe Premium Roast Decaf Coffee K-Cup Pods, Net Wt. 29 oz (823g), compare it against the product description and identifying codes (Best By 17 NOV 2026 LA hh:mm PL070 5321 or 5322 Batch Number: 5101564894 Material Number: 5000358463 ASIN: B07GCNDL91) before using it.

The general guidance for a matching product is to stop using it and follow the instructions in the official FDA recall notice, which may include a repair, replacement, refund, or safe disposal. When in doubt, contact Keurig DR Pepper, Inc. or your local health authority.

About this recall

This recall was distributed in TN. RecallRadar summarizes recall information from public FDA data to make it easier to understand. We are an independent service and are not affiliated with the FDA or any government agency, so please always refer to the official source for the authoritative record — and note the “last synced” date shown on this page, since recall details can change over time.

Full recall details

Status
Terminated
Date reported
February 4, 2026
Recall started
December 6, 2025
Distributed in
TN
What was recalled
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.
Why it was recalled (as stated by the FDA)
Product is labeled as decaf, but might contain caffeine.
How to identify the affected product
Best By 17 NOV 2026 LA hh:mm PL070 5321 or 5322 Batch Number: 5101564894 Material Number: 5000358463 ASIN: B07GCNDL91
Amount recalled
960 cartons (84 pods/carton)

What you can do

Check whether any product you have matches the description and codes above. If it does, stop using it and follow the instructions in the official recall notice. When in doubt, contact the company or your local health authority.

Quick answers

Why was McCafe Premium Roast Decaf Coffee K-Cup Pods, Net Wt. 29 oz (823g) recalled?+

According to the FDA: Product is labeled as decaf, but might contain caffeine.

How serious is this recall?+

Class II — moderate. Using this product might cause a temporary or medically reversible health problem. The chance of serious harm is low.

What should I do if I have McCafe Premium Roast Decaf Coffee K-Cup Pods, Net Wt. 29 oz (823g)?+

Compare your product against the description and identifying codes on this page. If it matches, stop using it and follow the instructions in the official recall notice — this usually means returning it for a refund or discarding it. When in doubt, contact the company or your local health authority.

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View the official FDA record

Opens the U.S. Food and Drug Administration (FDA) data for this recall.

Recall number: H-0419-2026. Information last synced from the FDA on July 5, 2026.