Old Europe Cheese, Inc.
Complete recall history across all FDA and CPSC categories — 10 total recalls
Old Europe Cheese, Inc. appears in recall records across 1 category. This page consolidates all FDA food, drug, and medical device enforcement actions, plus CPSC consumer product recalls associated with this company. Recall data is sourced from openFDA and CPSC public databases.
Food Recalls (10)
FDA food safety enforcement actions by Old Europe Cheese, Inc.
| Date | Product | Reason | Class |
|---|---|---|---|
| Sep 28, 2022 | Reny Picot 6.5 lb Brie-dbl cr¿me w/Peppercorn, whole wheel no UPC; Reny Pico... | potential contamination with Listeria monocytogenes | Class I |
| Sep 28, 2022 | BLACK BEAR 6 lb Black Bear Wheel no UPC BLOCK AND BARREL 2.2 lb Block and Ba... | potential contamination with Listeria monocytogenes | Class I |
| Sep 28, 2022 | Reny Picot 11 oz Apple Baked Brie UPC 033421500811 | potential contamination with Listeria monocytogenes | Class I |
| Sep 28, 2022 | JOAN OF ARC 2.2 lb Joan of Arc Peppercorn Wheel no UPC | potential contamination with Listeria monocytogenes | Class I |
| Sep 28, 2022 | TASTE OF INSPIRATION 8 oz Brie - w/Herb center layer, rounds UPC 725439802567 | potential contamination with Listeria monocytogenes | Class I |
| Sep 28, 2022 | FREDERICKS 8 oz Brie - triple cr¿me, rounds UPC 708820301214 FRESH THYME 8 o... | potential contamination with Listeria monocytogenes | Class I |
| Sep 28, 2022 | LA BONNE VIE 11 oz Cranberry Baked Brie UPC 820581678821; Reny Picot 11 oz Cr... | potential contamination with Listeria monocytogenes | Class I |
| Sep 28, 2022 | Reny Picot 11 oz Fig Baked Brie UPC 033421053119 | potential contamination with Listeria monocytogenes | Class I |
| Sep 28, 2022 | LA BONNE VIE 7 oz Brie - dbl cr¿me w/Herbs, wedges, foil wrapped UPC 8205816... | potential contamination with Listeria monocytogenes | Class I |
| Sep 28, 2022 | Reny Picot 8 oz Baked Brie, Plain UPC 033421050088 Mexideli 12 oz Baked Brie,... | potential contamination with Listeria monocytogenes | Class I |
Frequently Asked Questions
A high number of recalls does not necessarily indicate that a company is unsafe. Large manufacturers that produce thousands of products across multiple categories will statistically appear in recall databases more frequently. What matters more is the severity of each recall (Class I being the most serious), the speed of response, and whether the company proactively identified and addressed the issue. Companies with robust safety programs often catch problems earlier.
Food, drug, and medical device recall data comes from the FDA's openFDA enforcement database, which contains all FDA enforcement reports. Consumer product recall data comes from the U.S. Consumer Product Safety Commission (CPSC). Both sources are public government databases that are updated regularly. RecallCheck aggregates these sources to provide a unified view of a company's recall history.
The FDA classifies recalls into three categories. Class I is the most serious — there is a reasonable probability that use of or exposure to the product will cause serious adverse health consequences or death. Class II means the product may cause temporary or medically reversible health problems, or the probability of serious consequences is remote. Class III is the least serious — the product is unlikely to cause adverse health consequences. CPSC product recalls do not use this classification system.
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