Dilettante Mocha Cafe brand Light Ephemere Bulk Truffles, perishable, sold in individual pieces out of retail display ca
Summary
The FDA issued a Class III for Dilettante Mocha Cafe brand Light Ephemere Bulk Truffles, perishable, sold in in by Dilettante Chocolates Inc. Reason: The firm's retail placard posted on display case declares cream and butter in the ingredients statement, but the placard declares "Contains Dairy" onl.
Details
Source
Food Recall
External ID
F-1406-2023
Action Date
2023-08-23
Status
Terminated
Category
food
Product Description
Dilettante Mocha Cafe brand Light Ephemere Bulk Truffles, perishable, sold in individual pieces out of retail display cases. The display placard declares cream and butter in the ingredients statement, but the Contains statement declares "Contains: Dairy". Bulk truffle boxes sent to retail stores contains correct label: "***Dilettante Mocha Cafe Light Ephemere Bulk Truffles*** UPC 10083 15045***Contains: Milk***Dilettante Mocha Cafe, Tukwila, WA 98188, dilettantemochacafe.com".
Lot/Code Info: Manufactured 6/2/2023 and bulk case includes best by date 11/2/23.
Quantity Affected: firm did not provide
Reason for Recall
The firm's retail placard posted on display case declares cream and butter in the ingredients statement, but the placard declares "Contains Dairy" only.
Distribution
Distributed to firm's retail store locations in WA
Type: Voluntary: Firm initiated
Recall Initiated: 2023-07-06
Company
Tukwila, WA
Context & Analysis
This is a Class III recall. Class III recalls involve products unlikely to cause adverse health consequences, but that violate FDA regulations.
This was one of 85 food recalls issued in the same week, part of 204 food-related FDA actions this month.
Dilettante Chocolates Inc has 16 FDA actions in our database, including 16 recalls.
Frequently Asked Questions
What is a Class III recall?
A Class III recall involves products that are unlikely to cause adverse health effects but violate FDA labeling or manufacturing regulations.
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 (Dilettante Chocolates Inc) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Dilettante Chocolates Inc have FDA actions?
Dilettante Chocolates Inc has 16 FDA actions in our database, including 16 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "F-1406-2023" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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