Keurig Dr Pepper — FDA Recall History & Enforcement Records
Data Notice: Recall frequency varies by category and firm size; data is comparative and may not indicate actual brand safety or quality. See Methodology.
As of July 16, 2026, Keurig Dr Pepper has 9 recorded FDA food enforcement actions in the openFDA database. Their most recent recall was on 6 Dec 2025. Keurig Dr Pepper is categorized under Beverages based on their predominant recall history.
Recall activity over time for Keurig Dr Pepper
How serious are Keurig Dr Pepper recalls?
FDA recall classifications by severity
Full FDA recall history for Keurig Dr Pepper
All 9 FDA enforcement actions sourced from openFDA · Sorted by date, most recent first
| Date | Product | Reason | Class & Status |
|---|---|---|---|
| 6 Dec 2025Official FDA Notice | McCafe Premium Roast Decaf Coffee K-Cup Pods, Net Wt. 29 oz (823g), packaged as an 84-count carton, UPC 043000073438. Di | Product is labeled as decaf, but might contain caffeine. | Class IITerminated |
| 3 Feb 2023Official FDA Notice | Celestial Seasonings Mandarin Orange Spice Herbal Tea in K-cup pods; packed 24 to a box | Product contains black tea, resulting in caffeine being undeclared. | Class IITerminated |
| 9 Dec 2021Official FDA Notice | Diet Snapple Tea Peach Tea 16 oz. packaged in PET bottle. Expiration Date: February 5, 2022. UPC single bottles: 0 76183 | Product labeled to be Diet and Zero Sugar in the ingredient statement may contain sugar due to an production error. | Class IITerminated |
| 14 Oct 2021Official FDA Notice | Target Good & Gather Coconut Pineapple Sparkling Water 8 pack of 12 oz. cans UPC can: 0 85239 04059 1, UPC outer carton | The company has received off flavor and off aroma complaints identified with the recalled lot. After analysis it was found that the products contained | Class IITerminated |
| 14 Oct 2021Official FDA Notice | 7UP Zero Sugar Lemon Lime Soda 12 pack of 12 oz. can UPC Cardboard Wrap Code: 7800001181 UPC Can Code: 0780790 | The company has received off flavor and off aroma complaints identified with the recalled lot. After analysis it was found that the products contained | Class IITerminated |
| 14 Oct 2021Official FDA Notice | Polar Black Cherry Premium Seltzer 12 pack of 12oz cans UPC Cardboard Wrap Code: 7153700228, UPC Can Code: 7153700110 | The company has received off flavor and off aroma complaints identified with the recalled lot. After analysis it was found that the products contained | Class IITerminated |
| 14 Oct 2021Official FDA Notice | Target Good & Gather Mixed Berry Sparkling Water 8 pack of 12 oz. cans UPC can: 0 85239 11516 9, UPC outer Carton (8 pac | The company has received off flavor and off aroma complaints identified with the recalled lot. After analysis it was found that the products contained | Class IITerminated |
| 13 Sep 2021Official FDA Notice | Rc Cola 12 Oz (355 mL) packaged in an aluminum can 12 can to a pack | Consumer complaints of off flavor and aroma | Class IITerminated |
| 25 Aug 2020Official FDA Notice | Newman’s Own Organics, Newman’s Special Decaf Medium Roast, Ground Coffee, 10 oz. | Roast ground coffee packed in Newman s Own Organics special decaffeinated packaging contained regular non-organic Coffee. | Class IITerminated |
Where have Keurig Dr Pepper recalls occurred?
States affected across all recorded FDA enforcement actions
Where does this recall data come from?
Verification required: FoodRecallFinder.com cannot verify the safety of individual food products in your possession. Always verify the current recall status at FDA.gov before disposing of or consuming a product.
Data sourced from the FDA Recall Enterprise System via openFDA API. This information is for educational purposes only and does not constitute health or legal advice. FoodRecallFinder.com is not affiliated with or endorsed by the U.S. Food and Drug Administration.
To determine if your specific product is affected, verify that the brand name, product description, lot number, UPC code, and date range all match the recall details exactly. When in doubt contact the recalling firm or visit FDA.gov.
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