Duc De Coeur Camembert Cheese Croquettes Frozen NET WT 9 OZ (256g) UPC 2023 8391 Packaged in a cardboard cartons.
Summary
The FDA issued a Class II for Duc De Coeur Camembert Cheese Croquettes Frozen NET WT 9 OZ (256g) UPC 2023 8391 by Lidl US TRADING. Reason: Possible contamination with Listeria monocytogenes.
Details
Source
Food Recall
External ID
F-0794-2024
Action Date
2024-01-31
Status
Terminated
Category
food
Product Description
Duc De Coeur Camembert Cheese Croquettes Frozen NET WT 9 OZ (256g) UPC 2023 8391 Packaged in a cardboard cartons.
Lot/Code Info: BBD 27 OCTOBER 2024
Quantity Affected: 5,400 units
Reason for Recall
Possible contamination with Listeria monocytogenes
Distribution
Distribution centers and retails stores in MD, NC, VA, GA, SC, PA, NJ, NY and Washington D.C.
Type: Voluntary: Firm initiated
Recall Initiated: 2024-01-04
Company
Arlington, 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 85 food recalls issued in the same week, part of 204 food-related FDA actions this month.
Lidl US TRADING has 15 FDA actions in our database, including 15 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 TRADING) 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 TRADING have FDA actions?
Lidl US TRADING has 15 FDA actions in our database, including 15 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "F-0794-2024" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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