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FDA Issues Coffee Recall Across 15 States Due to Mislabeled Caffeine Content
The U.S. Food and Drug Administration (FDA) has issued a voluntary recall of Our Family Traverse City Ground Coffee, following reports of mislabeled caffeine content in the product. The recalled coffee is labeled as decaffeinated but actually contains detectable levels of caffeine.
A total of 692 cases of the affected products were shipped to 15 states across the country, including Colorado, Iowa, Illinois, Indiana, Kansas, Kentucky, Mississippi, Minnesota, North Carolina, North Dakota, Nebraska, Ohio, South Dakota, Wisconsin, and Wyoming. The recalled product comes in 12-ounce bags with a best-buy date of August 8, 2025.
The FDA classified this recall as a Class II, indicating that use or exposure to the violative product may cause temporary or reversible adverse health consequences. This is not a trivial issue, given the potential impact on consumers who rely on decaf coffee for its intended benefits.
It’s essential to understand that caffeine can have several negative effects on the body, particularly in higher doses. Consumers who ingest caffeine, either intentionally or unintentionally, may experience symptoms such as jitters, nervousness, anxiety, insomnia, and dehydration. Long-term consumption of high amounts of caffeine can also lead to more severe health issues.
In this specific case, those who have consumed the mislabeled coffee may be at risk of experiencing these adverse effects due to the unexpected presence of caffeine. The FDA advises that individuals affected by this recall should monitor their blood pressure and heart rate closely, as increased caffeine consumption can exacerbate pre-existing conditions such as high blood pressure or heart disease.
For its part, Our Family has issued a statement acknowledging the issue and apologizing for any inconvenience caused. “We are committed to your health and safety, and we follow best practices to ensure the quality and safety of the products we sell,” the company said in a statement.
The FDA’s Class II recall is seen as an important move to protect public health, given the widespread use of coffee among millions of Americans. The agency urges consumers who have purchased the affected product to return it to their place of purchase for a full refund or replacement with a non-caffeinated alternative.
This incident serves as a critical reminder that even seemingly innocuous products can have unintended consequences when mislabeled or contaminated.
Source: https://www.forbes.com/sites/brucelee/2025/03/30/fda-coffee-recall-across-15-states-from-mislabeling-as-decaffeinated/
