Stop using nowFood recall · FDA · Published January 4, 2024
Lidl Camembert Cheese Croquettes Recall: Possible Listeria Contamination
Lidl recalls Duc De Coeur Camembert Cheese Croquettes frozen product due to possible Listeria monocytogenes contamination. Consumers should check UPC 2023 8391 for affected items.
“Lidl Camembert Cheese Croquettes Recall: Possible Listeria Contamination.” GovInfoNow, updated August 17, 2026. https://govinfonow.com/recall/9803-lidl-camembert-cheese-croquettes-recall-possible-listeria-contamination. Based on FDA recall #F-0794-2024 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-0794-2024%22&limit=1).
Lidl US TRADING is recalling Duc De Coeur Camembert Cheese Croquettes Frozen because of possible Listeria monocytogenes contamination, the FDA announced on Jan. 4, 2024. The firm recalled 5,400 units distributed in Maryland, North Carolina, Virginia, Georgia, South Carolina, Pennsylvania, New Jersey, New York and Washington D.C.
How to tell if you have it
Duc De Coeur Camembert Cheese Croquettes Frozen NET WT 9 OZ (256g) UPC 2023 8391
UPC 00000020238391
Best Before Date: 27 OCTOBER 2024
The hazard
The product may be contaminated with Listeria monocytogenes. The FDA classified the recall as Class II.
Context
GovInfoNow's records show Lidl US TRADING has 15 other recalls on record since Sept. 13, 2018. Other recent recalls of similar products include Markys Caviar Mon Sire Brie Cheese Recall (Aug. 25, 2026), Clover Hill Dairy Sharp Cheese Recall (June 1, 2026) and Clover Hill Dairy Mild Cheese Variety Recall (June 1, 2026).
How to tell if you have this one
Check for the UPC 2023 8391 on the cardboard carton packaging. The product was packaged in late October 2024.
Brand
Lidl
Product
Duc De Coeur Camembert Cheese Croquettes Frozen NET WT 9 OZ (256g) UPC 2023 8391 Packaged in a cardboard cartons
Category
Food
Based on the official FDA remedy
What to do — step by step
Stop Using Now
Discard the recalled Duc De Coeur Camembert Cheese Croquettes frozen product immediately.
Where it went and when
Where it was distributed
Distributed in 8 states and D.C..
Listed by the agency
Not listed
FDA distribution: “Distribution centers and retails stores in MD, NC, VA, GA, SC, PA, NJ, NY and Washington D.C.” States read from FDA’s own wording; “not listed” means the notice does not name it.
States: District of Columbia, Georgia, Maryland, New Jersey, New York, North Carolina, Pennsylvania, South Carolina, Virginia.
Recall timeline
FDA terminated this recall 9 months after the firm started it.
1Firm started the recall
2FDA classified it Class II
3Published in FDA’s Enforcement Report
4FDA terminated the recall
Dates from the agency record only; steps without a date are left out.
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
Official source: FDA Recall #F-0794-2024 (January 4, 2024) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-0794-2024 to see it in context.
Plain-language summary written by qwen3:4b on August 17, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.