CLASS II Food recall · Reported 4 Feb 2026 · FDA Enforcement Report

McCafe Premium Roast Decaf Coffee K-Cup Pods recalled

Keurig DR Pepper is recalling McCafe Premium Roast Decaf Coffee K-Cup Pods, distributed in California, Indiana, Nevada. The recall was initiated on 6 Dec 2025 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codesBest By 17 NOV 2026 LA hh:mm PL070 5321 or 5322 Batch Number: 5101564894 Material Number: 5000358463 ASIN: B07GCNDL91
Quantity recalled960 cartons (84 pods/carton)

Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.

Recall details

Recall number
H-0419-2026
FDA event ID
98138
Recalling firm
Keurig DR Pepper, Knoxville, TN
Brand
McCafe
Classification
Class II
Status
Terminated
Recall initiated
6 Dec 2025
FDA classified
23 Jan 2026
Reported
4 Feb 2026
Type
Voluntary: Firm initiated
Customers notified by
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Reason category
Packaging Defects
Product category
Coffee

Timeline

6 Dec 2025Recall initiated by company
23 Jan 2026Classified by FDA+48 days
4 Feb 2026Published in enforcement report+12 days

Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.

Reason for recall

Product is labeled as decaf, but might contain caffeine.

Packaging recalls include wrong labels, wrong products in the wrong bottle, missing leaflets, short-filled or empty capsules and seals that fail.

Product as listed by the FDA

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.

Where it was distributed

CA, IN, NV

CaliforniaIndianaNevada

Questions about this recall

Why was it recalled?

Product is labeled as decaf, but might contain caffeine.

Which lots are affected?

Best By 17 NOV 2026 LA hh:mm PL070 5321 or 5322 Batch Number: 5101564894 Material Number: 5000358463 ASIN: B07GCNDL91

Where was it sold?

CA, IN, NV

What should I do if I have it?

Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.

What does Class II mean?

Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.

Read the official FDA notice · Source record retrieved 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.

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