Lower riskFood recall · FDA · Published August 25, 2020
Newman's Own Organic Coffee Recall: Regular Coffee in Organic Packaging
Newman's Own recalls organic decaf coffee that contains regular non-organic coffee due to packaging mix-up. Consumers should check product codes and contact the company for details.
“Newman's Own Organic Coffee Recall: Regular Coffee in Organic Packaging.” GovInfoNow, updated October 4, 2026. https://govinfonow.com/recall/15192-newman-s-own-organic-coffee-recall-regular-coffee-in-organic. Based on FDA recall #F-1364-2020 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-1364-2020%22&limit=1).
The FDA announced on August 25, 2020, that Keurig Dr Pepper, Inc. is recalling Newman's Own Organics Newman's Special Decaf Medium Roast Ground Coffee, 10 oz., because the product was packed in decaffeinated packaging but contained regular non-organic coffee.
How to tell if you have it
Brand: Newman's Own
Product: Newman's Own Organics Newman's Special Decaf Medium Roast Ground Coffee, 10 oz.
SKU: 099555395662
Best by Date: 21 JUN 2021 and 22 JUN 2021
Quantity: 7050 - 10 oz. bags
Distribution: New York, Connecticut, Pennsylvania, Maine, Massachusetts
The hazard
The roast ground coffee was packed in Newman's Own Organics special decaffeinated packaging but contained regular non-organic coffee.
Context
GovInfoNow's records show Keurig Dr Pepper, Inc. has one other recall on record since December 6, 2025, including the McCafe Premium Roast Decaf K-Cup Pods recall from that date which cited a caffeine hazard. Other recent recalls of similar products include the Gimme Coffee Decaf Pods Recall (November 24, 2025) and the Horizon Organic Lowfat Milk Recall (March 11, 2026).
How to tell if you have this one
Check for the bar code 099555395662 on the packaging. The product was sold with best by dates of June 21, 2021, or June 22, 2021.
Brand
Newman's Own
Category
Food
Based on the official FDA remedy
What to do — step by step
Check Product Details
Look for the bar code 099555395662 and best by dates of June 21 or 22, 2021.
Where it went and when
Where it was distributed
Distributed in 5 states.
Listed by the agency
Not listed
FDA distribution: “New York, Connecticut, Pennsylvania, Maine, Massachusetts” States read from FDA’s own wording; “not listed” means the notice does not name it.
States: Connecticut, Maine, Massachusetts, New York, Pennsylvania.
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 #F-1364-2020 (August 25, 2020) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-1364-2020 to see it in context.
Plain-language summary written by qwen3:4b on October 4, 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.