FDA Recall of Mislabeled Coffee Remains Active Across 15 States

Consumers urged to verify purchases and return mislabeled Traverse City Cherry Decaf Light Roast Coffee for refunds or replacements.

The FDA has classified the recall of Traverse City Cherry Decaf Light Roast Coffee as Class II, indicating low risk of serious health consequences.
The recall affects 692 cases of 12-ounce packages mislabeled as decaffeinated but containing caffeine, posing risks to individuals avoiding caffeine.
Products were distributed in 15 states, including Colorado, Michigan, and Wisconsin, and feature a specific best-before date and UPC code.
SpartanNash, the distributor, confirmed all affected products were removed from shelves and destroyed before the FDA's classification.
Consumers are advised to check packaging details and return affected products to stores for refunds or replacements.