Class IITerminated in FDA datasetRecall initiated Dec 6, 2025

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

Recalling firm: Keurig DR Pepper, Inc.

Why it was recalled

Product is labeled as decaf, but might contain caffeine.

Historical recall record. This is not a new recall announcement. “Terminated” describes the FDA recall process; it does not certify that an individual package is safe. FDA termination date: May 21, 2026.

Check your package

Compare the exact product and package details with the label you have.

ProductMcCafe 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.
Package size29 oz
UPC043000073438

FDA code information

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

Match the product, package size, and code together. A missing match does not guarantee safety.

Full FDA record and distribution details

Original 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.

Extracted codes and context

TypeCode / valueContext
UPC043000073438af 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.
batch5101564894Best By 17 NOV 2026 LA hh:mm PL070 5321 or 5322 Batch Number: 5101564894 Material Number: 5000358463 ASIN: B07GCNDL91

Original FDA recall reason

Product is labeled as decaf, but might contain caffeine.

Recall details

Recall number
H-0419-2026
Event ID
98138
FDA status
Terminated
Initiated
Dec 6, 2025
Reported
Feb 4, 2026
Classified
Jan 23, 2026
Terminated
May 21, 2026
Quantity
960 cartons (84 pods/carton)
Location
Knoxville, TN, United States
Initiation type
Voluntary: Firm initiated
Notification
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit

Where it was distributed

CA, IN, NV

FDA source record · H-0419-2026

Data updated September 16, 2026. View official FDA data ↗

Follow official FDA and manufacturer guidance.