Vemondo Vegan Coconut & Cocoa Non-Dairy Dessert Cones 4-3.7 fl ounces (110 mL) cones UPC 4 056489 468646
Summary
The FDA issued a Class II for Vemondo Vegan Coconut & Cocoa Non-Dairy Dessert Cones 4-3.7 fl ounces (110 mL) c by Lidl US Operations, LLC. Reason: Undeclared milk allergen.
Details
Source
Food Recall
External ID
F-0394-2022
Action Date
2022-01-19
Status
Terminated
Category
food
Product Description
Vemondo Vegan Coconut & Cocoa Non-Dairy Dessert Cones 4-3.7 fl ounces (110 mL) cones UPC 4 056489 468646
Lot/Code Info: L 04HC Expiration Date: 04.08.23
Quantity Affected: 729 units (total)
Reason for Recall
Undeclared milk allergen
Distribution
Distributed to retail stores in MD, VA, and PA.
Type: Voluntary: Firm initiated
Recall Initiated: 2021-12-10
Company
Fredericksburg, 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 146 food recalls issued in the same week, part of 204 food-related FDA actions this month.
Lidl US Operations, LLC has 2 FDA actions in our database, including 2 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 (Lidl US Operations, LLC) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Lidl US Operations, LLC have FDA actions?
Lidl US Operations, LLC has 2 FDA actions in our database, including 2 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "F-0394-2022" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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