Food recall

Massimo Zanetti Beverage USA recall: COFFEE ROASTERS Our Family TRAVERSE CITY CHERRY ARTIFICIALLY FLAVORED DECAF LIGHT ROAST GROUND COFFEE NET WT 12 OZ...

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.... The FDA's reason: “Mislabeling. A portion of the production of Our Family Traverse City Ground Coffee was mislabeled as decaffeinate.” The FDA classified it Class II: it could cause temporary or minor harm. The company began the recall voluntarily on March 13, 2025, and the FDA first listed it in its Enforcement Report of April 2, 2025. The FDA has closed the recall: it found the company did all it reasonably could to remove or correct the product.

How serious

Class II

It could cause temporary or minor harm

Why

Labeling, packaging or manufacturing problems

Status

Terminated

Closed July 1, 2025

The recall

Company
Massimo Zanetti Beverage USA (Suffolk, VA)
Reason, in FDA's words
“Mislabeling. A portion of the production of Our Family Traverse City Ground Coffee was mislabeled as decaffeinate.”
Where it was sold
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
Recall began
, by the company
FDA classified it
First in an FDA Enforcement Report
FDA event number
96499

The product recalled

As the FDA describes them, with the codes that tell whether a package is part of the recall.

  • F-0666-2025 Class II

    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

    Codes: BEST BEFORE 080325 V 15:37 C

    Quantity: 692cs/6/12oz bags

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Source and notes

U.S. Food and Drug Administration, Enforcement Reports (openFDA food recall data) (Public domain (U.S. government work); source U.S. Food and Drug Administration, openFDA), data as of April 2, 2025.

Each week the FDA lists the recalls it has classified in its Enforcement Report, often weeks after the company announced the recall, so a month with five weekly reports tends to count more. Each recall counts once, however many products it covers, in the month FDA first listed it. Class I means the food could cause serious harm or death, Class II temporary or minor harm, and Class III is unlikely to harm anyone. Meat, poultry and most egg products are recalled by the U.S. Department of Agriculture, not the FDA, and aren't included. For what to do with a recalled product, see the FDA's recalls page.