FDA Issues Recall for McCafé Decaf K-Cups Due to Unexpected Caffeine Levels
FOX Business reporter Lauren Simonetti shares the latest on the rise in coffee prices on ‘Mornings with Maria.’
The U.S. Food and Drug Administration (FDA) has announced a voluntary recall of over 80,000 McCafé Premium Roast Decaf Coffee K-Cup pods distributed by Keurig Dr Pepper. This recall was initiated after the company discovered that some pods labeled as decaffeinated may actually contain regular, full-caffeine coffee.
According to the FDA, the recall affects approximately 960 cartons, each containing 84 coffee pods, totaling 80,640 individual K-Cups. Keurig Dr Pepper began the recall on December 6, 2025, but the FDA classified it as a Class II recall on January 23, 2026.
A spokesperson for Keurig Dr Pepper confirmed to FOX Business that “outreach to impacted consumers already happened directly in December.” They added, “Consumers were encouraged to contact Keurig Consumer Care directly at (866) 901 2739 to arrange for product replacement.”
ENERGY DRINKS FACE NEW RESTRICTIONS ABROAD: COULD THE US BE NEXT IN LINE?
Keurig voluntarily recalled more than 80,000 McCafé decaf K-Cup pods because they may contain caffeine. (Daniel Acker/Bloomberg via Getty Images / Getty Images)
A Class II recall indicates that the use or exposure to the product may lead to temporary or medically reversible adverse health consequences, although the likelihood of serious health effects is considered remote. The FDA clarified that the recall was prompted by a labeling error and not due to any safety concerns regarding the coffee itself.
The affected McCafé Premium Roast Decaf Coffee K-Cup pods were sold through a single retailer and distributed in California, Indiana, and Nevada.
SUPPLEMENT SOLD AT GAS STATIONS SPARKS HEALTH FEARS AS PEOPLE REPORT ADDICTION SYMPTOMS
The coffee pods that are being recalled are Keurig’s McCafé decaf K-Cup pods. They were sold in California, Nevada and Indiana. (iStock)
The affected products are packaged in 84-count cartons, weighing a net total of 29 ounces (823 grams). They can be identified by the UPC code 043000073438, a best-by date of November 17, 2026, batch number 5101564894, material number 5000358463, and ASIN B07GCNDL91, as noted on the FDA’s website.
While consuming these products does not pose a significant health risk for most individuals, it could lead to adverse effects for those sensitive to caffeine or advised to avoid it.
SUPPLEMENT SOLD AT GAS STATIONS SPARKS HEALTH FEARS AS PEOPLE REPORT ADDICTION SYMPTOMS
The FDA said the coffee is just mislabeled – not unsafe to consume. (Sarah Silbiger/Getty Images / AP Newsroom)
Consumers who purchased the recalled pods are advised to dispose of them or return them to the retailer for a full refund or replacement. The recall is ongoing, and as of now, no illnesses or injuries related to the product have been reported.
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In a statement to FOX Business, Keurig Dr Pepper emphasized, “At Keurig Dr Pepper, we are committed to the highest standards of safety and quality in the products we produce and distribute. In cooperation with the FDA, we initiated a voluntary recall of a limited number of 84-count boxes of McCafe Premium Roast Decaf coffee K-Cup pods, sold through a single retail partner, as the coffee may contain regular caffeinated coffee.” They also noted that all consumers who purchased this product were notified directly by the retailer and provided with next steps regarding a replacement product. All remaining impacted products with the retailer have been returned to the company.
FOX Business reporter Lauren Simonetti shares the latest on the rise in coffee prices on ‘Mornings with Maria.’
The U.S. Food and Drug Administration (FDA) has announced a voluntary recall of over 80,000 McCafé Premium Roast Decaf Coffee K-Cup pods distributed by Keurig Dr Pepper. This recall was initiated after the company discovered that some pods labeled as decaffeinated may actually contain regular, full-caffeine coffee.
According to the FDA, the recall affects approximately 960 cartons, each containing 84 coffee pods, totaling 80,640 individual K-Cups. Keurig Dr Pepper began the recall on December 6, 2025, but the FDA classified it as a Class II recall on January 23, 2026.
A spokesperson for Keurig Dr Pepper confirmed to FOX Business that “outreach to impacted consumers already happened directly in December.” They added, “Consumers were encouraged to contact Keurig Consumer Care directly at (866) 901 2739 to arrange for product replacement.”
ENERGY DRINKS FACE NEW RESTRICTIONS ABROAD: COULD THE US BE NEXT IN LINE?
Keurig voluntarily recalled more than 80,000 McCafé decaf K-Cup pods because they may contain caffeine. (Daniel Acker/Bloomberg via Getty Images / Getty Images)
A Class II recall indicates that the use or exposure to the product may lead to temporary or medically reversible adverse health consequences, although the likelihood of serious health effects is considered remote. The FDA clarified that the recall was prompted by a labeling error and not due to any safety concerns regarding the coffee itself.
The affected McCafé Premium Roast Decaf Coffee K-Cup pods were sold through a single retailer and distributed in California, Indiana, and Nevada.
SUPPLEMENT SOLD AT GAS STATIONS SPARKS HEALTH FEARS AS PEOPLE REPORT ADDICTION SYMPTOMS
The coffee pods that are being recalled are Keurig’s McCafé decaf K-Cup pods. They were sold in California, Nevada and Indiana. (iStock)
The affected products are packaged in 84-count cartons, weighing a net total of 29 ounces (823 grams). They can be identified by the UPC code 043000073438, a best-by date of November 17, 2026, batch number 5101564894, material number 5000358463, and ASIN B07GCNDL91, as noted on the FDA’s website.
While consuming these products does not pose a significant health risk for most individuals, it could lead to adverse effects for those sensitive to caffeine or advised to avoid it.
SUPPLEMENT SOLD AT GAS STATIONS SPARKS HEALTH FEARS AS PEOPLE REPORT ADDICTION SYMPTOMS
The FDA said the coffee is just mislabeled – not unsafe to consume. (Sarah Silbiger/Getty Images / AP Newsroom)
Consumers who purchased the recalled pods are advised to dispose of them or return them to the retailer for a full refund or replacement. The recall is ongoing, and as of now, no illnesses or injuries related to the product have been reported.
CLICK HERE TO DOWNLOAD THE FOX BUSINESS APP
In a statement to FOX Business, Keurig Dr Pepper emphasized, “At Keurig Dr Pepper, we are committed to the highest standards of safety and quality in the products we produce and distribute. In cooperation with the FDA, we initiated a voluntary recall of a limited number of 84-count boxes of McCafe Premium Roast Decaf coffee K-Cup pods, sold through a single retail partner, as the coffee may contain regular caffeinated coffee.” They also noted that all consumers who purchased this product were notified directly by the retailer and provided with next steps regarding a replacement product. All remaining impacted products with the retailer have been returned to the company.
