Recall record at a glance
| Official record | F-0116-2023 |
|---|---|
| Category | Food Recalls |
| Classification | Class I |
| FDA record status | Terminated |
| Recalling firm | Old Europe Cheese, Inc. |
| Report date | Nov 9, 2022 |
| Recall initiation date | Sep 28, 2022 |
| Quantity | 146495 pieces |
| Location | Benton Harbor, MI, United States |
Official product description
FREDERICKS 8 oz Brie - triple cr¿me, rounds UPC 708820301214 FRESH THYME 8 oz Brie - triple cr¿me, rounds UPC 841330111987 HEINEN 8 oz Brie - triple cr¿me, rounds UPC 020601418028 JOAN OF ARC 6.5 lb Joan of Arc Triple Creme Wheel no UPC JOAN OF ARC 8 oz Joan of Arc Triple Creme Wheel UPC 711565129104 LA BONNE VIE 8 oz Brie - triple cr¿me, rounds UPC 820581678746 MARKET 32 8 oz Brie - triple cr¿me, rounds UPC 41735052858 METROPOLITAN 6.5 lb Metropolitan Wheel no UPC METROPOLITAN 8 oz Metropolitan Wheel UPC 711565007679 PRESTIGE 8 oz Brie - triple cr¿me, rounds UPC 021140033635 Reny Picot 2.2 lb Brie - triple cr¿me, whole wheel ST ROCCO no UPC Reny Picot 6.5 lb Brie - triple cr¿me, whole wheel no UPC Reny Picot 8 oz Brie - triple cr¿me, rounds - ST ROCCO UPC 133421027865 Reny Picot 8 oz Brie - trpl cr¿me, wedges, saran wrap RW - ST ROCCO no UPC ST RANDEAUX 8 oz Brie - triple cr¿me, rounds UPC 636625003548 TASTE OF INSPIRATION 8 oz Brie - triple cream, rounds UPC 725439802550 TASTE OF INSPIRATION 8 oz Brie - triple cr¿me, rounds UPC 725439999731
Why the product was recalled
potential contamination with Listeria monocytogenes
Distribution information
AR AZ CA CO FL GA IL IN LA MA MD MI MN MO NC NJ NY OH OR PA TX UT VA WA WI and Mexico
How to read the classification
FDA Class I indicates a situation in which there is a reasonable probability that use of or exposure to the product will cause serious adverse health consequences or death. The classification shown here comes directly from the FDA enforcement record.
Additional record details
Recall type: Voluntary: Firm initiated. Initial notification: Telephone.
What to do next
If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.
About this record
Recall Lookup USA preserves the most complete source information successfully retrieved. We do not create missing facts or infer affected lots or VINs. The official record may still change, so use the identifier above when verifying current instructions.
FDA source limitation: openFDA enforcement reports are a reference dataset, not a live public-alert or recall-lifecycle service. FDA notes that enforcement-report status may not be updated after classification. Confirm current actions with the FDA, recalling firm or appropriate healthcare professional when relevant.