Coffee Recall - Mislabeled Decaf Poses Health Risks in 15 States

Coffee Recall - Mislabeled Decaf Poses Health Risks in 15 States

A voluntary recall has been issued for 692 cases of ground coffee due to mislabeling. The affected product is Our Family-branded Traverse City Cherry artificially flavored decaf light roast ground coffee. This coffee was incorrectly labeled as decaffeinated, which can be dangerous for those avoiding caffeine for health reasons. The recall affects 15 states and was initiated by Massimo Zanetti Beverage USA.

• The recall involves 12-ounce bags with UPC 0 70253 11080 1 and a "BEST BEFORE" code of 080325 V 15:37 C.

• The FDA classified this recall as Class II, indicating a risk but not serious health consequences for most consumers.

• Consumers with caffeine sensitivities, medical conditions, or pregnancy may experience negative effects from consuming the mislabeled coffee.

• The recall was first reported on March 13 and officially classified by the FDA on March 25.

Addressing this issue is crucial for consumer safety. Mislabeling can lead to serious health risks, especially for vulnerable groups. Awareness about caffeine content in decaf products is essential for those who must avoid it. This recall highlights the importance of accurate labeling in food products to protect public health.

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