FDA recalls ground coffee
FDA recalls ground coffee: The FDA recalled ground coffee that was incorrectly labeled as decaffeinated and distributed across 15 states in the U.S. The affected product, Our Family Traverse City Cherry Decaf Light Roast Ground Coffee, contained caffeine despite its decaf labeling, potentially posing risks to those with caffeine sensitivity.
Thousands of Pounds of Coffee Pulled from Shelves: Coffee Recalled
FDA coffee recall
The FDA is recalling ground coffee due to mislabeling concerns. The recall affects hundreds of 12 oz bags sold in Colorado, Iowa, Illinois, Indiana, Kansas, Kentucky, Missouri, Minnesota, North Carolina, North Dakota, Nebraska, Ohio, South Dakota, Wisconsin, and Wyoming.FDA recalls ground coffee
The recall was voluntarily initiated on March 13 by Massimo Zanetti Beverage USA, a major U.S. coffee supplier, in cooperation with its distributor, SpartanNash.
coffee recalled fda coffee recall: FDA Classifies Recall as “Category II”
The FDA recalls ground coffee under a “category II” classification, meaning that consuming the mislabeled product could lead to temporary or medically reversible health issues. Consumers relying on decaf coffee for health reasons are urged to avoid the affected batches.
FDA recalls ground coffee Company Ensures Consumer Safety: FDA recalls ground coffee
Our Family clarified that no other coffee products under its brand were impacted by the recall.
“We prioritize the health and safety of our consumers and adhere to strict quality standards. We apologize for any inconvenience this may have caused,” the company stated.
As of now, Massimo Zanetti Beverage USA and SpartanNash have not provided additional comments regarding the recall.
