Recall of Ground Coffee in 15 States Due to Incorrect Caffeine Labeling

The U.S. Food and Drug Administration (FDA) has announced the recall of ground coffee products sold across 15 states, following the discovery that these items may have been incorrectly labeled as decaffeinated. This recall affects hundreds of 12-ounce bags of Our Family Traverse City Cherry Decaf Light Roast Ground Coffee.

The affected products were distributed in the states of Colorado, Iowa, Illinois, Indiana, Kansas, Kentucky, Missouri, Minnesota, North Carolina, North Dakota, Nebraska, Ohio, South Dakota, Wisconsin, and Wyoming. It is important to note that no other products from the company are included in this recall.

Massimo Zanetti Beverage U.S., one of the largest suppliers in the coffee industry, initiated this voluntary recall on March 13. In a statement regarding the situation, the company emphasized its commitment to consumer health and safety, asserting that it adheres to best practices to ensure product quality. They expressed regret for any inconvenience this situation may have caused to consumers.

The FDA has categorized this event as a Category II recall. This classification indicates that the use or exposure to the affected products may lead to temporary or medically reversible adverse health effects.

As of the latest reports, neither Massimo Zanetti nor SpartanNash, the distributor of the coffee, has responded to media inquiries concerning the recall.

Consumers are encouraged to check their pantry for the recalled product and to discard it or return it to the place of purchase for a refund. The FDA has advised that individuals who may have consumed the product should monitor their health and consult a medical professional if they experience any negative effects.

For further guidance on caffeine consumption and its health impacts, resources are available from the American Medical Association.