FDA Recalls Coffee in 15 States Over Mislabeled Caffeination

Massimo Zanetti Beverage USA voluntarily recalls 692 cases of coffee mislabeled as decaffeinated, with no serious health consequences reported so far.

The FDA has classified the recall as Class II, indicating a low likelihood of serious health risks but potential temporary or reversible effects.
The recall involves 12-ounce bags of Our Family Traverse City Cherry Decaf Light Roast Ground Coffee with a best-before date of August 3, 2025, and a specific UPC code.
692 cases of mislabeled coffee were distributed to retail stores and distribution centers across 15 states, including Colorado, Michigan, and Wisconsin.
Consumers sensitive to caffeine are advised to return the affected product for a refund or replacement, as other Our Family Coffee products remain unaffected.
Massimo Zanetti Beverage USA and the FDA continue to monitor the situation, with no reports of adverse health effects to date.