Coffee Recall in 15 States Due to Decaf Mislabeling
Key Insights
Product: Our Family Traverse City Cherry Artificially Flavored Decaf Light Roast Ground Coffee (12-ounce bags).
Identifier: UPC 0 70253 11080 1, Code: "BEST BEFORE 080325 V 15:37 C".
Issue: Product labeled "Decaf" contains regular caffeinated coffee.
Affected States: CO, IA, IL, IN, KS, KY, MI, MN, NC, ND, NE, OH, SD, WI, WY.
Quantity: 692 cases recalled.
FDA Classification: Class II - may cause temporary or medically reversible health issues, serious consequences unlikely.
Why this matters: Accidental caffeine consumption can cause adverse effects like irregular heartbeat, high blood pressure, anxiety, or insomnia, particularly for pregnant individuals, those with heart conditions or high blood pressure, people on certain medications, or those with caffeine sensitivity.
In-Depth Analysis
The recall was initiated via phone on March 13, 2025, by Massimo Zanetti Beverage USA after the mislabeling was discovered, and formally classified by the FDA on March 25, 2025. The coffee was distributed by SpartanNash Company of Grand Rapids, Michigan, primarily to retail stores in the Midwestern and Great Lakes regions under its "Our Family" store brand.
While the FDA's Class II classification suggests a lower risk of severe harm, the presence of caffeine can be problematic for vulnerable groups. The FDA notes that even standard decaf coffee contains small amounts of caffeine (2-15mg per 8oz cup). However, consuming regular coffee unknowingly could lead to significantly higher caffeine intake.
Dr. Luciana Torquati, a registered nutritionist, highlighted potential amplified effects in children (restlessness, anxiety, sleep issues) and risks during pregnancy due to slower caffeine clearance and potential impact on fetal heart rate and maternal blood pressure. People with existing high blood pressure or specific medical conditions exacerbated by caffeine, as well as those highly sensitive to it, could experience palpitations, anxiety, or sleep disruption even with smaller doses.
FAQs
Q: Which specific coffee product is under recall?
A: The recall affects 12-ounce bags of Our Family Traverse City Cherry Artificially Flavored Decaf Light Roast Ground Coffee with UPC 0 70253 11080 1 and the code "BEST BEFORE 080325 V 15:37 C".
Q: What is the reason for the recall?
A: The product was incorrectly labeled as decaffeinated but contains regular caffeinated coffee.
Q: What should I do if I purchased this coffee?
A: If you need to avoid caffeine, do not consume the product. You can contact the manufacturer, Massimo Zanetti Beverage USA, for a refund.
Key Takeaways
Check your coffee supply for the specific Our Family product details (brand, flavor, UPC, best by code).
If you possess the recalled product and need to avoid caffeine for health reasons (pregnancy, heart condition, sensitivity, medication interaction), refrain from consuming it.
Contact Massimo Zanetti Beverage USA to inquire about a refund for the affected product.
Be aware that even correctly labeled decaf products contain trace amounts of caffeine.
Discussion
This recall highlights the importance of accurate food labeling, especially for ingredients like caffeine that can affect health. Have you ever been affected by a food recall or mislabeling?
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Sources & References
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