F-Bombs Cookie Dough Truffles: 12 ounce plastic packaging, plastic packaging is packed into 4x4x2 cardboard boxes. UPC 8
Summary
The FDA issued a Class II for F-Bombs Cookie Dough Truffles: 12 ounce plastic packaging, plastic packaging is by Fox Confections LLC. Reason: Undeclared FD&C Yellow #5 and Yellow #6.
Details
Source
Food Recall
External ID
F-1537-2023
Action Date
2023-09-27
Status
Terminated
Category
food
Product Description
F-Bombs Cookie Dough Truffles: 12 ounce plastic packaging, plastic packaging is packed into 4x4x2 cardboard boxes. UPC 850036018032
Lot/Code Info: Product No. 01803
Quantity Affected: 150 (12oz) packages
Reason for Recall
Undeclared FD&C Yellow #5 and Yellow #6
Distribution
Distributed to 90 retail locations in Illinois and Ohio
Type: Voluntary: Firm initiated
Recall Initiated: 2023-08-31
Company
Mentor, OH
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 52 food recalls issued in the same week, part of 204 food-related FDA actions this month.
Fox Confections LLC has 7 FDA actions in our database, including 7 recalls.
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 (Fox Confections LLC) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Fox Confections LLC have FDA actions?
Fox Confections LLC has 7 FDA actions in our database, including 7 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "F-1537-2023" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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