Class IITerminatedVoluntary: Firm initiated
Massimo Zanetti Beverage USA: food recall F-0666-2025
Massimo Zanetti Beverage USA of Suffolk, VA recalled COFFEE ROASTERS Our Family TRAVERSE CITY CHERRY ARTIFICIALLY FLAVORED DECAF LIGHT ROAST GROUND COFFEE NET WT 12 OZ… Reason: Mislabeling. A portion of the production of Our Family Traverse City Ground Coffee was mislabeled as decaffeinate. The FDA listed it as Class II in its Enforcement Report dated Apr 2, 2025; distribution: Colorado, Iowa, Illinois, Indiana, Kansas, Kentucky, Michigan, Minnesota, North Carolina, North Dakota, Nebraska, Ohio, South Dakota, Wisconsin, Wyoming.
Record status as published: Terminated (terminated Jul 1, 2025). openFDA data last updated Oct 21, 2026.
Have this product? Check FDA.gov and your retailer. This page reproduces an FDA Enforcement Report record and is not a public alert. Look for the firm's recall notice on the FDA's recalls page, or ask the store where you bought it what to do. If you think you got sick from a food, contact a health care provider.
Recall details
- Product
- 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
- Product quantity
- 692cs/6/12oz bags
- Reason for recall
- Mislabeling. A portion of the production of Our Family Traverse City Ground Coffee was mislabeled as decaffeinate.
- Codes, lots and dates on the package
- BEST BEFORE 080325 V 15:37 C
- 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
- Recalling firm
- Massimo Zanetti Beverage USA, Suffolk, VA
- Classification
- Class II — the FDA uses this class for a situation in which using or being exposed to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious adverse health consequences is remote.
- Voluntary or mandated
- Voluntary: Firm initiated
- How the firm first notified customers
- Telephone
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Dates
| Event | Date |
|---|---|
| Recall initiated by the firm | Mar 13, 2025 |
| Classified by the FDA | Mar 25, 2025 |
| Published in the Enforcement Report | Apr 2, 2025 |
| Terminated | Jul 1, 2025 |
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Sources
- U.S. Food and Drug Administration, openFDA food enforcement reports, recall number F-0666-2025 (openFDA record). Data provided by the U.S. Food and Drug Administration (https://open.fda.gov).
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