“McCafe Premium Roast Decaf K-Cup Pods May Contain Caffeine.” GovInfoNow, updated August 17, 2026. https://govinfonow.com/recall/6912-mccafe-premium-roast-decaf-k-cup-pods-may-contain-caffeine. Based on FDA recall #H-0419-2026.
Keurig DR Pepper, Inc. recalled McCafe Premium Roast Decaf Coffee K-Cup Pods because the product is labeled as decaf but might contain caffeine, according to the FDA. The Food and Drug Administration announced the recall on December 6, 2025.
How to tell if you have it
McCafe Premium Roast Decaf Coffee K-Cup Pods
Net Wt. 29 oz (823g)
84-count carton
UPC 043000073438
Best By 17 NOV 2026 LA hh:mm PL070 5321 or 5322 Batch Number: 5101564894 Material Number: 5000358463 ASIN: B07GCNDL91
The hazard
The product is labeled as decaf, but might contain caffeine. The recall involves 960 cartons distributed in California, Indiana, and Nevada.
Context
GovInfoNow's records show Keurig DR Pepper, Inc. has one other recall on record since August 25, 2020, involving Newman's Own Organic Coffee packed in decaffeinated packaging that contained regular coffee. Other recent recalls of similar products include Gimme Coffee Decaf Pods Recall (November 24, 2025) and Lost and Found Energy Sour Gummy Bear Recall (December 2, 2025).
How to tell if you have this one
Check for the UPC code 043000073438 on the carton. The product is a 29 oz (823g) 84-count carton of McCafe Premium Roast Decaf Coffee K-Cup Pods.
Brand
Keurig
Product
McCafe Premium Roast Decaf Coffee K-Cup Pods, Net Wt. 29 oz (823g), packaged as an 84-count carton, UPC 043000073438
Category
Food
Based on the official FDA remedy
What to do — step by step
Check Product Details
Look for the UPC 043000073438 on the carton to identify affected products.
Where it went and when
Where it was distributed
Distributed in 3 states.
Listed by the agency
Not listed
FDA distribution: “CA, IN, NV” States read from FDA’s own wording; “not listed” means the notice does not name it.
States: California, Indiana, Nevada.
Recall timeline
FDA terminated this recall 5 months after the firm started it.
1Firm started the recall
2FDA classified it Class II
3Published in FDA’s Enforcement Report
4FDA terminated the recall
Dates from the agency record only; steps without a date are left out.
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
Official source: FDA Recall #H-0419-2026 (December 6, 2025)
Plain-language summary written by qwen3:4b on August 17, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.