Ground Coffee Recalled By FDA Over Mislabeled Packaging

Yahoo

29-03-2025

A popular coffee brand has recalled over 600 cases of ground coffee after the packages were incorrectly labeled as decaffeinated.
The U.S. Food and Drug Administration (FDA) reports that parent company Massimo Zanetti Beverage USA issued a voluntary recall earlier this month for 692 cases of Our Family Traverse City 12-oz ground coffee bags, specifically the Traverse City Cherry Artificially Flavored Decaf Light Roast Ground Coffee.
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According to the FDA, the recall is due to a mislabeling error, after "a portion of the production of Our Family Traverse City Ground Coffee was mislabeled as decaffeinate."
The affected bags, with an expiration date of Aug. 3, 2025, were sent to distribution centers and retail locations across 15 states: Colorado, Iowa, Illinois, Indiana, Kansas, Kentucky, Missouri, Minnesota, North Carolina, North Dakota, Nebraska, Ohio, South Dakota, Wisconsin and Wyoming.
The initial recall was first issued by the company on March 13, and has since been classified by the FDA as a Class II risk, which the organization describes as "a situation in which use of, or exposure to, a violative product may cause temporary or medically reversible adverse health consequences or where the probability of serious adverse health consequences is remote."
As of the time of publication, this recall is still ongoing.
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