Massimo Zanetti Beverage USA Recall: Mislabeling. A portion of the production of Our Family Traverse City Ground Coffee was mislabeled as decaffeinate.
United States
TerminatedClass II
- Company
- Massimo Zanetti Beverage USA
- Product
- COFFEE ROASTERS Our Family TRAVERSE CITY CHERRY ARTIFICIALLY…
- Recall date
- March 13, 2025
- Terminated
- July 1, 2025
- Source
- FDA
Reason for recall
Mislabeling. A portion of the production of Our Family Traverse City Ground Coffee was mislabeled as decaffeinate.
- - Recall initiated
- - Reported by source
- - Recall terminated
| Product description | UPC | Quantity | Lot / code information |
|---|---|---|---|
| COFFEE ROASTERS Our Family TRAVERSE CITY CHERRY ARTIFICIALLY FLAVORED DECAF LIGHT ROAST GROUND COFFEE NET WT 12 OZ (340g) UPC 0 70253 11080 1 DISTRIBUTED BY THE SPARTANNASH COMPANY GRAND RAPIDS, MI 49518 | Not published in this source record | 692cs/6/12oz bags | BEST BEFORE 080325 V 15:37 C |
Distribution
- Product was shipped to distribution centers and retail stores in the following states: CO
- IA
- IL
- IN
- KS
- KY
- MI
- MN
- NC
- ND
- NE
- OH
- SD
- WI and WY
Official source record
- Agency
- FDA
- Dataset
- FDA Food Enforcement (Recalls)
- Recall number
- F-0666-2025
- Event ID
- 96499
- Status
- Terminated
- Classification
- Class II
- Company
- Massimo Zanetti Beverage USA
- Product description
- COFFEE ROASTERS Our Family TRAVERSE CITY CHERRY ARTIFICIALLY FLAVORED DECAF LIGHT ROAST GROUND COFFEE NET WT 12 OZ (340g) UPC 0 70253 11080 1 DISTRIBUTED BY THE SPARTANNASH COMPANY GRAND RAPIDS, MI 49518
- Quantity
- 692cs/6/12oz bags
- Reason
- Mislabeling. A portion of the production of Our Family Traverse City Ground Coffee was mislabeled as decaffeinate.
- Recall initiation date
- March 13, 2025
- Report date
- April 2, 2025
- Classification date
- Not published in this source record
- Termination date
- July 1, 2025
- Distribution pattern
- Product was shipped to distribution centers and retail stores in the following states: CO, IA, IL, IN, KS, KY, MI, MN, NC, ND, NE, OH, SD, WI and WY
- UPC, lot, and code information
- BEST BEFORE 080325 V 15:37 C
- Voluntary or mandated
- Voluntary: Firm initiated
- Initial notification method
- Telephone
- Source last updated
- Not tracked separately from the Public Health Trace retrieval date below
- Public Health Trace retrieval date
Responsible company: Massimo Zanetti Beverage USA
A map highlighting the states named in the source's distribution description.
Shading reflects state-level totals only, as published by the source. It does not imply county-level or point-level precision.
| State | Distributed |
|---|---|
| Colorado | 1 |
| Iowa | 1 |
| Illinois | 1 |
| Indiana | 1 |
| Kansas | 1 |
| Kentucky | 1 |
| Michigan | 1 |
| Minnesota | 1 |
| North Carolina | 1 |
| North Dakota | 1 |
| Nebraska | 1 |
| Ohio | 1 |
| South Dakota | 1 |
| Wisconsin | 1 |
| Wyoming | 1 |
States shown are extracted from the source's free-text distribution description above; a narrative description (e.g. "distributed nationwide") may not list individual states to extract.
Where this information comes from
View FDA enforcement record -- the specific openFDA record this summary was built from.
This record comes from FDA's Enforcement Report database. Not every Enforcement Report record has a separate FDA.gov recall-announcement page.
FDA Enforcement Reports -- FDA's general, official recall and enforcement information.
Technical source data
View raw source data -- the machine-readable record this page's information was built from.
Retrieved by Public Health Trace:
Frequently asked questions
What does a Class II mean?
A situation in which use of or exposure to a product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote.
Is this recall still active?
According to FDA, this recall's status is "Terminated." Always confirm the current status using the source links below, since status can change after Public Health Trace last retrieved this record.
What should I do if I have this product?
Follow the instructions published by the responsible agency (see the source links below) -- recall guidance (e.g. dispose of the product, return it for a refund, or check for a specific lot number) varies by recall and is set by that agency, not by Public Health Trace.
Where can I find more official information?
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