If you’re one of the millions of Americans who start their day with a cup of coffee—especially decaf—you might want to double-check what’s in your pantry. The U.S. Food and Drug Administration (FDA) has issued a recall for nearly 700 cases of Massimo Zanetti Beverage USA’s decaf coffee due to mislabeling.
What’s Wrong With the Coffee?
On March 25, 2025, the FDA announced that certain 12-ounce bags of Our Family-branded Traverse City Cherry artificially flavored decaf light roast ground coffee were incorrectly labeled as “decaffeinated” when they actually contained caffeine. The recalled coffee was distributed across 15 states, including Ohio, Colorado, Kansas, North Carolina, and Kentucky.
Here’s what to look for:
- UPC: 0 70253 11080 1
- Best Before: 080325 V 15:37 C
The FDA categorized this as a Class 2 recall, meaning the product could cause temporary or reversible health issues, though serious risks are considered low.
Why This Could Be Dangerous
Decaf coffee is expected to have 97% of its caffeine removed, making it a safe choice for people who are sensitive to caffeine. However, for those with health conditions like high blood pressure, heart disease, anxiety disorders, or irregular heart rhythms, unexpected caffeine consumption could lead to severe effects like:
- Rapid heart rate
- Increased anxiety or panic attacks
- Seizures or strokes (in extreme cases)
What You Should Do
If you purchased this coffee, stop using it immediately and return it to the store for a refund. To stay updated on product recalls, check the FDA’s Recalls, Market Withdrawals, & Safety Alerts webpage.
Your morning coffee should be a source of comfort—not a health risk. Stay informed and check those labels!