RecallHawk
Class II Recall

McCafe Premium Roast Decaf Coffee K-Cup Pods, Net Wt. 29 oz (823g), packaged as an 84-count carton, UPC 043000073438. Di

Keurig DR Pepper, Inc.

Summary

The FDA issued a Class II for McCafe Premium Roast Decaf Coffee K-Cup Pods, Net Wt. 29 oz (823g), packaged as by Keurig DR Pepper, Inc.. Reason: Product is labeled as decaf, but might contain caffeine..

Details

Source

Food Recall

External ID

H-0419-2026

Action Date

2026-02-04

Status

Terminated

Category

food

Product Description

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.

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

Quantity Affected: 960 cartons (84 pods/carton)

Reason for Recall

Product is labeled as decaf, but might contain caffeine.

Distribution

CA, IN, NV

Type: Voluntary: Firm initiated

Recall Initiated: 2025-12-06

Company

Context & Analysis

This is a Class II recall. Class II recalls indicate that use of or exposure to the product may cause temporary or medically reversible health consequences, or that the probability of serious consequences is remote.

This was one of 34 food recalls issued in the same week, part of 204 food-related FDA actions this month.

Frequently Asked Questions

What is a Class II recall?

A Class II recall means the product may cause temporary or medically reversible adverse health consequences, or the probability of serious adverse consequences is remote. Consumers should discontinue use.

What should I do if I have this product?

Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (Keurig DR Pepper, Inc.) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does Keurig DR Pepper, Inc. have FDA actions?

This is the only FDA action we have on record for Keurig DR Pepper, Inc. in our database.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "H-0419-2026" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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