FDA Issues Recall: Popular 'Decaf' Coffee Found to Contain Regular Caffeine
The FDA has issued a Class II recall for Our Family's Traverse City Cherry Decaf Ground Coffee due to incorrect labeling. The product, marketed as decaffeinated, likely contains regular caffeine levels, potentially putting sensitive consumers at risk.
Affected Product Details:
- Product Code: 0 70253 11080 1
- Best By Date: August 3, 2025
- Size: 12 oz packages
- Distribution: 692 cases across 15 states including Michigan, Illinois, Indiana, Colorado, Ohio, and Kentucky
Health Implications:
- Regular coffee contains approximately 96mg of caffeine per cup
- Decaf typically contains only 1-2mg of caffeine
- This mislabeling poses risks for:
- Caffeine-sensitive individuals
- Pregnant women
- People with heart conditions
What to Do:
- Check your product code and best-by date
- Dispose of affected products immediately
- Monitor for symptoms if consumed
- No official refund guidance has been issued yet by SpartanNash or FDA
The FDA classifies this as a moderate risk recall, meaning while not likely to cause permanent damage, it could lead to temporary or medically reversible adverse health effects.
Consumers who purchased this product believing it was decaffeinated should immediately discontinue use and verify their package details against the recall information.
No serious incidents have been reported yet, but the potential health risks, especially for sensitive individuals, make this recall significant for consumer safety.