Massimo Zanetti Beverage USA Coffee Recall- If this is what’s been on your mind lately, we’re here to spill all the beans.
Massimo Zanetti Beverage USA Coffee Recall is actually a significant food safety warning that deals with at least a thousand coffee bags across 15 states. This recall of Massimo Zanetti Beverage USA coffee dealt with improper labeling of product packaging. It led to decaf items carrying full-strength caffeine. For health reasons, many of us choose not to take caffeine. Massimo Zanetti Beverage USA issued the recall as soon as the issue gained traction.
The following extended guide will walk you through the event comprehensively.
- What products were recalled?.
- Proactive steps one can take to address the issue.
- How the recall played out in a larger context of food safety and labeling.
Therefore, if these are a few things that you want to know, then keep on reading this blog till the end…
What Was Recalled: Product Codes And Scope of the Problem

The product, particularly being recalled by Massimo Zanetti Beverage USA, is coffee under the brand name “Our Family”. Consumers had purchased this coffee under the assurance that they were buying a decaffeinated product.
Identifying The Affected Coffee
You should compare your coffee bag with the following lot details. Do not consume any product matching the following information:
- Brand and Full Name: Our Family Traverse City Cherry Artificially Flavored Decaf Light Roast Ground Coffee.
- Package Size: Product is sold in 12-oz bags.
- Universal Product Code (UPC): Check code 0 70253 11080 1 on container.
- Important Lot Code: The date code on the affected product reads “BEST BEFORE 080325 V 15:37 C”.
Distribution And Scale
A leading share of the product in the Massimo Zanetti Beverage USA coffee recall was sold by SpartanNash Company of Grand Rapids, Michigan.
- Quantity: The recall involves about 692 cases. To put that in perspective, that is 4,152 individual bags of ground coffee.
- States Affected: Distribution reached retail in the following 15 U.S. states: Colorado, Iowa, Illinois, Indiana, Kansas, Kentucky, Michigan, Minnesota, North Carolina, North Dakota, Nebraska, Ohio, South Dakota, Wisconsin, and Wyoming.
What Is A Class II Recall: The Classification In Massimo Zanetti Beverage USA Coffee Recall

It was recalled by Massimo Zanetti Beverage USA on 13th March 2025. The Food and Drug Administration categorized it as a Class II Recall on 25th March 2025 for the Massimo Zanetti Beverage USA Coffee Recall.
A Class II recall just means that product exposure may cause temporary or medically reversible adverse health consequences, and that the probability of serious harm is remote. In this categorization, however, mislabeled coffee does present a very real and quantifiable health danger to sensitive persons.
Why This Recall Is A Health Hazard
People drink decaf coffee because they want control over the amount of caffeine they are ingesting. The reasons could be medical, pregnancy, or even sensitivity of the person. The error in recalling the Massimo Zanetti Beverage USA coffee takes away that important choice.
Health Effects On The Vulnerable Group
The simple point surrounds the Massimo Zanetti Beverage USA Coffee Recall. Several hazardous side effects have been associated with full-dose caffeine consumption when decaf is expected; this is mainly for some vulnerable populations:
- Heart Patients: Unsolicited caffeine speeds up the heart, causes palpitations, and high blood pressure that can become dangerous for heart patients, according to Prevention.
- Pregnancy and Lactation: CAFFEINE crosses the placenta and is excreted in significant amounts into breast milk. High, unintentional dosing is dangerous to the mother and the developing baby.
In a person sensitive to caffeine or with anxiety, it could provoke a lot of anxiety, jitters, tremors, or insomnia.
Interactions with other medications: Caffeine can interact negatively with various types of medications, including but not limited to certain antibiotics, asthma drugs, and heart medicines, according to MedlinePlus.
Decaf Standards: Mislabelled Coffee
The term “decaffeinated” is highly regulated. One standard 8-ounce cup of regular brewed coffee contains about 95 mg to over 200 mg of caffeine.
Legal Standard for Decaf: The law demands that a minimum of 97% caffeine should be removed in decaffeination. Only about 2–7 mg of residual caffeine remains in decaf per standard serving.
The coffee at the center of the Massimo Zanetti Beverage USA coffee recall contains full caffeine levels. Thus, this means that its drinkers have had up to roughly 20 to 100 times the caffeine that they anticipated, having drunk it.
Consumer Action Guide: What You Need To Do
If you think your bag of coffee could be one of the lots from the Massimo Zanetti Beverage USA coffee recall, don’t waste a minute. Your health is more important.
Step-by-Step Check
- Locate Your Coffee: Locate any 12-ounce bags of Our Family Traverse City Cherry Artificially Flavored Decaf Light Roast Ground Coffee in your pantry.
- Code Check UPC verified: 0 70253 11080 1 “BEST BEFORE” date 080325 V 15:37 C
- Discuss and Act: If the codes match, it’s part of the Massimo Zanetti Beverage USA coffee recall.
The following steps will protect you, besides helping you to get compensated.
- Disposal Considerations Waste Disposal: Dispose of product immediately, or seal in container and return to place of purchase for refund.
- Refund/Replacement: Call the store where you purchased the coffee. They will give a complete refund or replacement. Seek medical consultation immediately, according to the Cleveland Clinic, in case either you or someone in your household has ingested the coffee and shows symptoms of severe anxiety, heart-pounding, or dizziness.
- Broader Context: Labeling, Trust, and Accountability
Recall of Massimo Zanetti Beverage USA coffee points out more than a single incident to critical factors that need improvement within the chain of food supply.
Read Also: The Great Ginger Deception: The Ginger Ale Lawsuit Explained
How Common Is The Incident Of Mislabeling?
Mislabeling factors, especially of caffeine, are also one of the well-known concerns in the food industry. As much as the coffee industry works towards high-quality control, errors may arise at every stage, from blending to packaging.
FDA continuously monitors these incidents, emphasizing that appropriate labeling cannot be compromised for consumer safety.
The event thus reminds all the manufacturing companies that strict quality checks must be performed.
The Role Of Quality Control And Massimo Zanetti Beverage USA
Most consumers are of the opinion that Massimo Zanetti Beverage USA has handled the matter of recall quite responsibly.
There was almost instant voluntary recall when the internal discovery of the mislabelling error took place. Although the importance of a proper quality assurance process still stays. The mislabeling error means caffeinated and decaffeinated beans or packaging mixed somewhere on the production line.
This must be a central focus of the company’s corrective action. Consumer trust depends on absolute transparency and corrective actions that prevent future mix-ups.
The Erosion Of Brand Trust
For an international supplier like Massimo Zanetti Beverage USA, this kind of mistake will only destroy the confidence of the consumer. Consumers rely on decaf labels for safe consumption. If these labels cannot be trusted, brand loyalty crumbles in an instant. It would take very apparent commitment to stringent QA processes for companies to regain consumer faith.
Expert Views: How To Stay Safe And Informed
Health experts attribute this to the reason that consumers, especially for the decaf coffee products, need to be very alert.
Safe Limits of Caffeine Consumption
The FDA says that up to 400 mg of caffeine per day is okay for all healthy adults. However, for the sensitive groups, including pregnant women, people with cardiac issues, and for children, this number decreases.
We suggest that you always discuss your caffeine intake with a healthcare professional. After all, underlying medical conditions are not to be taken lightly.
Tips For Buying Coffee Responsibly- Check All Details
Check These Out First:
• Product ID: Note the exact brand, code, and date to check your own coffee.
• Health Hazards: No more than a Class II medical hazard for people sensitive to caffeine.
• Decaf Standards: Know the critical difference between real decaf and the misleadingly-named product.
• Follow-up Actions: Seek an explanation regarding the refund and/or coffee replacement from that recall.
While buying any special product, ensure the brand name, the product name, and the clear “decaffeinated” label.
- Buy from trusted housefronts/retailers: Buy only from traceable distributors who maintain decent traceability.
- Recalls Monitoring: If you want to get more information on such recalls, you can go through the FDA’s Recall database and check out the news updates on the topic.
Read Also: Chobani Lawsuit: Legal Implications And Consumer Ramifications
Frequently Asked Questions (FAQs):
The Massimo Zanetti Beverage USA coffee recall requires immediate attention from consumers. It was like a wake-up call for both consumers and manufacturers regarding health and safety.
Well, it all started when the company officials found an internal mislabeling error. This led to caffeinated coffee being labelled as decaffeinated. The company immediately called for a voluntary recall.
Always buy from very established brands, and never take a package home without clear “decaffeinated” labeling. Also, look for the roaster’s contact information and the “best by” date. More importantly, sign up to receive email or text alerts from the FDA or food safety news sites so you will be promptly warned about any recalls.
At this time, the Massimo Zanetti Beverage USA coffee recall is strictly limited to the specific product, size, UPC, and lot code (“BEST BEFORE 080325 V 15:37 C”) of the “Our Family Traverse City Cherry Artificially Flavored Decaf Light Roast Ground Coffee.” No other Our Family brand products, nor any products from Massimo Zanetti Beverage USA, are included in this particular recall.
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