In a significant development that highlights the critical role of accurate labeling in the food and beverage industry, the U.S. Food and Drug Administration (FDA) has issued a Class II recall for a flavored ground coffee product distributed across 15 U.S. states. Health risks potentially affected a part of consumers who purposefully choose to stay away from caffeine because manufacturers labeled the Our Family product as decaffeinated although its content included regular amounts of caffeine.

Massimo Zanetti Beverage USA Coffee Recall: The Coffee in Question

The major issue functionally related to the recall includes:

• Product Name: Our Family Traverse City Cherry-Flavored Decaf Light Roast Ground Coffee  

• Packaging: 12-ounce bags Customers originally believed the product was decaffeinated despite it having regular caffeine levels.  

• UPC Code: 0 70253 11080 1

• Best By Dates: August 3, 2025, or August 8, 2025 (depending on sources)

The recall affected 692 product cases representing a grand total of 4,152 individual bags. The affected products do not represent a short run sold in local stores. The wide geographical reach means packages with this problem could be located in kitchen cabinets from different parts of the country.

Where the Product Was Sold

The distributor managed nationwide coffee distribution reaching retailers operating throughout Colorado, Iowa, Illinois, Indiana, Kansas, Kentucky, Missouri, Minnesota, North Carolina, North Dakota, Nebraska, Ohio, South Dakota, Wisconsin and Wyoming.

The extensive chain of distribution that used supermarkets alongside small retail outlets necessitated swift action from government authorities and consumer population alike.

Why This Recall Matters

At first glance, a caffeine mix-up might seem trivial. But to people with specific medical needs, mislabeling caffeine as decaf can be serious.

Here’s who could be affected:

• Heart disease patients who undergo restrictions on stimulant use require special attention.  

• People who have hypertension face a risk of developing elevated heart rate.  

• Pregnant women, who are often advised to limit caffeine

• Caffeine-sensitive individuals, prone to anxiety, jitteriness, or insomnia  

Consumers who rely on caffeine-free beverages would experience different levels of health effects when their misconception is discovered about undeclared caffeinated content in their coffee.

Customers face temporary medical consequences from this product which the FDA classified as Class II. The population needs to receive public warnings because the issue poses serious conditions for which companies must pull their products from stores.

Who Made the Coffee?

Massimo Zanetti Beverage USA stands as the leading coffee roasting and distribution company which produced the specific coffee batches. Massimo Zanetti Beverage USA took immediate voluntary recall actions through March 13, 2025 when they discovered the product labeling mistake.

The company teamed up with distribution partner SpartanNash to send proceedings which contained consumer apologies along with confirmations of their focus on quality safety.

The company actively works to address this situation and stop any health risks affecting consumers according to their statement.

This safety measure specifically targets only the cherry-flavored decaf ground coffee that carries the UPC code 0 70253 11080 1 with Best By dates of either August 3 or August 8, 2025.

What Should Consumers Do?

Consumers who purchased cherry-flavored decaf ground coffee under Our Family need to perform the following steps:

1. The bag contains a UPC code which reads 0 70253 11080 1.

2. Check the Best By label on the product package between August 3 and August 8 of 2025.

3. Consumers need to refrain from drinking the package if it matches the provided information.

4. Visit the store to obtain a full refund together with an opportunity to select different products

Consumers need to use the FDA’s MedWatch Adverse Event Reporting Program to report both symptoms and any negative reactions they experience.

Public health reports show no incidents occur but the FDA together with the manufacturer advise consumers to be careful particularly for people with medical limitations.

Final Thoughts

Customer safety depends on manufacturers upholding strict quality control protocols as shown by the Massimo Zanetti Beverage USA Coffee Recall. The typical coffee drinker would consider this manufacturing setback not worth much attention. People who face serious illnesses would potentially need unexpected visits to their doctor or potentially worse conditions if they make the mistake of consuming this product. When you opt for ground coffee from a bag, look closely at the information on the label during your next purchase. And in this case, it could be the most important sip you never took.