FDA recall mislabeled decaf Recall Issued

FDA recall mislabeled decaf coffee The FDA recalled Our Family Traverse City Cherry Decaf Light Roast Ground Coffee after finding thousands mislabeled. The recall was issued on March 13, 2025, and affects products sold in 15 states.

States Impacted by the Coffee Recall

Consumers in the following states may have purchased the mislabeled coffee:

• Colorado
• Iowa
• Illinois
• Indiana
• Kansas
• Kentucky
• Missouri
• Minnesota
• North Carolina
• North Dakota
• Nebraska
• Ohio
• South Dakota
• Wisconsin
• Wyoming

Health Impact and Recall Classification

FDA recall mislabeled decaf The FDA classified the recall as Category II, indicating the product may cause temporary or reversible health effects. While the coffee does not pose a life-threatening risk, individuals with caffeine sensitivities or certain medical conditions should be cautious.

Company Response

Massimo Zanetti Beverage USA, one of the largest coffee suppliers in the country, voluntarily initiated the recall. The distributor, SpartanNash, has yet to provide a statement.

In a public statement, Our Family reassured customers

“We are committed to your health and safety, and we follow best practices to ensure the quality and safety of the products we sell. We apologize for any inconvenience this may have caused.”

How to Respond If Someone Remembers Your Coffee

Check the container for lot numbers linked to the recall if you have already purchased Our Family Traverse City Cherry Decaf Light Roast Ground Coffee. Consumers are urged to: Return the item to the retailer for a full refund.

Source: NBC News