Newman's Own Organics, Newman's Special Decaf Medium Roast, Ground Coffee, 10 oz.
FDA Recall Notice
Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-1364-2020.
Roast ground coffee packed in Newman s Own Organics special decaffeinated packaging contained regular non-organic Coffee.
Corrective Action (per FDA)
Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-1364-2020.
Recall terminated by FDA.
✅ What you should do
- Stop using the product if you own it.
- Check the model number, lot code, or sell-by date against the recall notice above.
- Contact Keurig Dr Pepper, Inc. or the retailer where you bought it for a refund, replacement, or repair.
- For the most current official instructions, visit the FDA recall page.
- If you've been hurt by this product, report the incident to FDA.
Consumer Contact (per FDA)
Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-1364-2020.
Keurig Dr Pepper, Inc.
About the U.S. Food and Drug Administration
The FDA regulates drugs, medical devices, food, cosmetics, and tobacco. Adverse event reports and recall notices are the main public safety signal.
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If you had a reaction, found contamination, or experienced a labeling problem with this product, report it to the FDA. The agency uses consumer reports to track emerging safety signals and trigger recalls.
Keurig Dr Pepper, Inc. Recall FAQ
Keurig Dr Pepper, Inc. is the subject of a beverages safety report: Newman's Own Organics, Newman's Special Decaf Medium Roast, Ground Coffee, 10 oz.. The notice was published on August 25, 2020 by the U.S. Food and Drug Administration (FDA). Approximately 7,050 units are potentially affected.