Keurig Recalls Over 80,000 McCafé Decaf K-Cup Pods Due to Labeling Error

Keurig Dr Pepper has initiated a recall of more than 80,000 McCafé Premium Roast Decaf Coffee K-Cup Pods due to a labeling error.

 

The affected products, labeled as decaffeinated, may contain caffeine, posing potential health risks to individuals sensitive to caffeine.

 

The recall encompasses 960 cartons, each containing 84 pods, totaling 80,640 units.

 

These were distributed in California, Indiana, and Nevada.

 

Consumers can identify the recalled products by the following details:

 

Best By Date: 17 NOV 2026

 

UPC Code: 043000073438

 

Batch Number: 5101564894

 

Material Number: 5000358463

 

ASIN: B07GCNDL91

 

The U.S. Food and Drug Administration (FDA) has classified this as a Class II recall, indicating that consumption may cause temporary or medically reversible adverse health consequences.

 

While the likelihood of serious health issues is remote, individuals with caffeine sensitivities should exercise caution.

 

Consumers who have purchased the affected products are advised to discontinue use immediately.

 

They should contact the retailer for a refund or replacement.

 

For further assistance, consumers can reach out to Keurig Dr Pepper directly.

 

This recall underscores the importance of accurate product labeling, especially for items consumed by individuals with specific dietary needs.

 

Consumers are encouraged to check their coffee supplies and ensure they are not affected by this recall.

 

For more information, visit the FDA's official website or contact Keurig Dr Pepper customer service.