"feve x DANDELION CHOCOLATE CHOCOLATE - COVERED COCOA NIBS 4 OUNCES 113 GRAMS" Black triangular box with gold lettering.
Summary
The FDA issued a Class II for "feve x DANDELION CHOCOLATE CHOCOLATE - COVERED COCOA NIBS 4 OUNCES 113 GRAMS" B by Dandelion Chocolate. Reason: Undeclared allergen - hazelnuts.
Details
Source
Food Recall
External ID
F-1486-2024
Action Date
2024-07-24
Status
Terminated
Category
food
Product Description
"feve x DANDELION CHOCOLATE CHOCOLATE - COVERED COCOA NIBS 4 OUNCES 113 GRAMS" Black triangular box with gold lettering. Black box contains cellophane bag.
Lot/Code Info: Batch number: FNDHI4C4
Quantity Affected: 372 units
Reason for Recall
Undeclared allergen - hazelnuts
Distribution
CA, NV No foreign distribution
Type: Voluntary: Firm initiated
Recall Initiated: 2024-06-20
Company
San Francisco, CA
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 47 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 (Dandelion Chocolate) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Dandelion Chocolate have FDA actions?
This is the only FDA action we have on record for Dandelion Chocolate in our database.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "F-1486-2024" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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