Recall Radar

Keurig DR Pepper recalls McCafe Premium Roast Decaf Coffee K-Cup Pods: label issue

February 4, 2026 · Keurig DR Pepper Class II

Class IIFDA’s middle class: use of the product may cause temporary or medically reversible adverse health consequences, or the chance of serious harm is remote.
Reason for the recallProduct is labeled as decaf, but might contain caffeine.

Find the official FDA enforcement report

Recall at a glance

Recalling company
Keurig DR Pepper
Location
Knoxville, TN
Reported by FDA
February 4, 2026
Recall started
December 6, 2025
Risk class
Class II
Status (latest data we have)
Terminated
Type
Voluntary: Firm initiated
Category
Beverages
Reason type
Labeling and quality

Is my product affected?

Compare your product’s name, size and lot or date codes with the list below. A recall usually covers only specific codes.

  • 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.
    Quantity: 960 cartons (84 pods/carton)
    Codes: Best By 17 NOV 2026 LA hh:mm PL070 5321 or 5322 Batch Number: 5101564894 Material Number: 5000358463 ASIN: B07GCNDL91

Where it was distributed

CA, IN, NV

What to do

If you have this product, check the codes above. FDA recall notices often tell consumers to stop eating the product and to return it or throw it away. Follow the company’s instructions and the official FDA information, and if you are unsure, do not eat it. If someone becomes ill after eating a recalled food, contact a healthcare professional. See FDA’s recalls and safety alerts for company announcements.

Frequently asked questions

What was recalled?

Keurig DR Pepper recalled 1 product, including McCafe Premium Roast Decaf Coffee K-Cup Pods, Net Wt. 29 oz (823g), packaged as an 84-count carton, UPC 043000073438. Distributed By….

Why was it recalled?

Product is labeled as decaf, but might contain caffeine.

What does Class II mean?

FDA’s middle class: use of the product may cause temporary or medically reversible adverse health consequences, or the chance of serious harm is remote.

Where was it sold or shipped?

CA, IN, NV

What should I do if I have this product?

Compare the product name, size and lot or date codes with the details on this page. FDA recall notices often tell you to stop eating the product and to return it or throw it away. Follow the company’s instructions and the official FDA information. If you are unsure, do not eat it.

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Sources

Data provided by the U.S. Food and Drug Administration (FDA) through openFDA, shown as published and not validated by this site. This site is independent and is not affiliated with or endorsed by FDA. It covers FDA-regulated foods; meat, poultry and egg products are regulated by USDA. Do not rely on this site for medical decisions: for health concerns contact a healthcare professional, and always follow the official notice and the company’s instructions. Terms and disclaimer.