COFFEE ROASTERS Our Family TRAVERSE CITY CHERRY ARTIFICIALLY FLAVORED DECAF LIGHT ROAST GROUND COFFEE NET WT 12 OZ (340g
Summary
The FDA issued a Class II for COFFEE ROASTERS Our Family TRAVERSE CITY CHERRY ARTIFICIALLY FLAVORED DECAF LIGH by Massimo Zanetti Beverage USA. Reason: Mislabeling. A portion of the production of Our Family Traverse City Ground Coffee was mislabeled as decaffeinate..
Details
Source
Food Recall
External ID
F-0666-2025
Action Date
2025-04-02
Status
Terminated
Category
food
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
Lot/Code Info: BEST BEFORE 080325 V 15:37 C
Quantity Affected: 692cs/6/12oz bags
Reason for Recall
Mislabeling. A portion of the production of Our Family Traverse City Ground Coffee was mislabeled as decaffeinate.
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
Type: Voluntary: Firm initiated
Recall Initiated: 2025-03-13
Company
Suffolk, VA
Context & Analysis
This is a Class II recall. Class II recalls indicate that use of or exposure to the product may cause temporary or medically reversible health consequences, or that the probability of serious consequences is remote.
This was one of 33 food recalls issued in the same week, part of 204 food-related FDA actions this month.
Frequently Asked Questions
What is a Class II recall?
A Class II recall means the product may cause temporary or medically reversible adverse health consequences, or the probability of serious adverse consequences is remote. Consumers should discontinue use.
What should I do if I have this product?
Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (Massimo Zanetti Beverage USA) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Massimo Zanetti Beverage USA have FDA actions?
This is the only FDA action we have on record for Massimo Zanetti Beverage USA in our database.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "F-0666-2025" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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