Food recalls by company
KEURIG DR PEPPER food recalls
The FDA has listed 6 food recalls by KEURIG DR PEPPER since its Enforcement Reports began in June 2012, the newest on February 4, 2026. 0 were Class I, the most serious kind. The most common reason: labeling, packaging or manufacturing problems (3).
Food recalls since 2012
6
Class I, the most serious
0
Newest
February 4, 2026
Every recall, newest first
By the date the FDA first listed each in its weekly Enforcement Report. Each recall's page lists every product, with the codes that tell whether a package is part of it.
2026 (1 recall)
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Class II Terminated
McCafe Premium Roast Decaf Coffee K-Cup Pods
Why: Labeling, packaging or manufacturing problems
“Product is labeled as decaf, but might contain caffeine.”
2023 (1 recall)
-
Class II Terminated
Celestial Seasonings Mandarin Orange Spice Herbal Tea in K-cup pods
Why: Other ingredient not on the label (sulfites, dyes...)
“Product contains black tea, resulting in caffeine being undeclared.”
2022 (1 recall)
-
Class II Terminated
Diet Snapple Tea Peach Tea 16 oz
Why: Labeling, packaging or manufacturing problems
“Product labeled to be Diet and Zero Sugar in the ingredient statement may contain sugar due to an production error.”
2021 (2 recalls)
-
Class II Terminated
Target Good & Gather Coconut Pineapple Sparkling Water 8 pack of 12 oz (4 products)
Why: Other ingredient not on the label (sulfites, dyes...)
“The company has received off flavor and off aroma complaints identified with the recalled lot. After analysis it was found that the products contained unlabeled sulfites.”
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Class II Terminated
Rc Cola 12 Oz (355 mL) packaged in an aluminum can 12 can to a pack
“Consumer complaints of off flavor and aroma”
2020 (1 recall)
-
Class II Terminated
Newman's Own Organics, Newman's Special Decaf Medium Roast, Ground Coffee
Why: Labeling, packaging or manufacturing problems
“Roast ground coffee packed in Newman s Own Organics special decaffeinated packaging contained regular non-organic Coffee.”
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Recalls are grouped by the company name the FDA lists as the recalling firm, so a company's other names, or a parent company's brands, may have pages of their own. A recall is listed once however many products it covers.
Source and notes
U.S. Food and Drug Administration, Enforcement Reports (openFDA food recall data) (Public domain (U.S. government work); source U.S. Food and Drug Administration, openFDA), data as of October 14, 2026.
Each week the FDA lists the recalls it has classified in its Enforcement Report, often weeks after the company announced the recall, so a month with five weekly reports tends to count more. Each recall counts once, however many products it covers, in the month FDA first listed it. Class I means the food could cause serious harm or death, Class II temporary or minor harm, and Class III is unlikely to harm anyone. Meat, poultry and most egg products are recalled by the U.S. Department of Agriculture, not the FDA, and aren't included. For what to do with a recalled product, see the FDA's recalls page.