The U.S. Food and Drug Administration (FDA) has issued a recall for thousands of pounds of ground coffee distributed across multiple states after discovering that caffeinated coffee was mislabeled as decaffeinated.
The recall, announced by Massimo Zanetti Beverage USA, affects 12-ounce bags of Our Family Traverse City Cherry Decaf Light Roast Ground Coffee. The mislabeled product was distributed in Colorado, Iowa, Illinois, Indiana, Kansas, Kentucky, Michigan, Minnesota, North Carolina, North Dakota, Nebraska, Ohio, South Dakota, Wisconsin, and Wyoming.
The FDA has classified this as a Class II recall, meaning the mislabeled product could cause temporary or medically reversible health effects. However, the likelihood of serious health consequences is considered low.
Consumers who purchased the affected coffee are advised to check their packaging and stop using the product if it is part of the recall.
Related topics:
- FDA Recalls International Delight Coffee Creamers Over Health Risks
- Botulism Risk Prompts Recall of 300 Canned Coffee Types Across the U.S.
- Recall Issued for JoyJolt Glass Coffee Mugs After Injury Reports