Recall of Mislabeled Decaffeinated Coffee

Introduction to the Recall

Bags of ground coffee that were mislabeled as decaffeinated were recalled in 15 states including Illinois, according to the Food and Drug Administration. This recall affects a significant number of consumers who may have purchased the product believing it to be decaffeinated.

Details of the Recall

692 cases of 12 ounce bags of Our Family Traverse Ground Coffee were being recalled after being mislabeled decaffeinated, the FDA stated in an enforcement report. The recall, which was voluntarily initiated by the Massimo Zanetti Beverage USA earlier this month, saw bags distributed and sold in Colorado, Iowa, Illinois, Indiana, Kansas, Kentucky, Missouri, Minnesota, North Carolina, North Dakota, Nebraska, Ohio, South Dakota, Wisconsin and Wyoming.

Affected States and Distribution

The coffee is distributed by the SpartanNash Company out of Grand Rapids, Michigan. The wide distribution across 15 states indicates a potential for significant impact on consumers who rely on decaffeinated products for health or preference reasons.

Classification of the Recall

A Class II recall was called, meaning that the coffee may cause temporary or medically reversible adverse health consequences with a remote chance of serious health concerns for those with medical conditions preventing them from having caffeine, according to the FDA. This classification underscores the importance of accurate labeling to protect consumer health.

Consumer Implications

Consumers who have purchased the mislabeled coffee and have medical conditions that require them to avoid caffeine should be aware of the potential risks. It is crucial for these individuals to monitor their health and seek medical advice if they have consumed the product and are experiencing adverse effects.

Conclusion

The recall of mislabeled decaffeinated coffee highlights the importance of rigorous quality control and labeling practices in the food industry. Consumers must be able to trust that the products they purchase are accurately represented. The FDA’s classification and the voluntary recall by the manufacturer are steps towards protecting public health, but it also serves as a reminder for consumers to be vigilant about the products they use.

FAQs

• Q: Which states are affected by the recall?
  • A: The recall affects 15 states including Colorado, Iowa, Illinois, Indiana, Kansas, Kentucky, Missouri, Minnesota, North Carolina, North Dakota, Nebraska, Ohio, South Dakota, Wisconsin, and Wyoming.
• Q: What is the reason for the recall?
  • A: The recall is due to the mislabeling of ground coffee as decaffeinated when it actually contains caffeine.
• Q: What should consumers do if they have purchased the recalled coffee?
  • A: Consumers, especially those with medical conditions that prevent them from consuming caffeine, should stop using the product and consult with a healthcare professional if they have concerns.
• Q: How was the recall initiated?
  • A: The recall was voluntarily initiated by the Massimo Zanetti Beverage USA.
• Q: What is the classification of the recall?
  • A: The recall is classified as a Class II recall, indicating that the product may cause temporary or medically reversible adverse health consequences.