FDA Recall United States OngoingHistorical recordClass I
Rizo Lopez Foods, Inc. dba Don Francisco Cheese
- Product
- Paneer (bulk)
- Published
- February 7, 2024
- Distribution
- U.S. distribution to the following: AR,…
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Policy version 2026-07-21, effective July 21, 2026.
United States
OngoingClass I
Listeria monocytogenes contamination.
| Product description | UPC | Quantity | Lot / code information |
|---|---|---|---|
| Cheddar Conventional (bulk) | Not published in this source record | PLU Batch ID 40456 1DZ-23307 40456 2DY-23307 40456 3DX-23307 40456 4CW-23307 40456 4DW-23307 40455 3EZ-23314 40455 4EY-23314 40456 1BX-23315 40456 2BW-23315 40456 3AZ-23315 40456 4BY-23315 40456 1DZ-23322 40456 2DY-23322 40456 3DX-23322 40456 4CW-23322 40456 1DZ-23335 40456 2DY-23335 40456 3DX-23335 40456 4CW-23335 40455 1DX-23342 40455 2DW-23342 40455 3DZ-23342 40455 4CY-23342 40456 1EX-23342 40456 2EW-23342 40456 3EZ-23342 40456 4DY-23342 40456 1DW-23349 40456 1EZ-23349 40456 2EY-23349 40456 3EX-23349 40456 1DW-23353 40456 2DZ-23353 40456 3DY-23353 40456 4CX-23353 40455 1DZ-24017 40455 2DY-24017 40455 3DX-24017 40455 4EW-24017 |
This recall shares FDA event ID 93814 with 9 other product entries in Public Health Trace.
FDA Recall United States OngoingHistorical recordClass I
FDA Recall United States OngoingHistorical recordClass I
FDA Recall United States OngoingHistorical recordClass I
FDA Recall United States OngoingHistorical recordClass I
FDA Recall United States OngoingHistorical recordClass I
FDA Recall United States OngoingHistorical recordClass I
FDA Recall United States OngoingHistorical recordClass I
FDA Recall United States OngoingHistorical recordClass I
FDA Recall United States OngoingHistorical recordClass I
Responsible company: Rizo Lopez Foods, Inc. dba Don Francisco Cheese
FDA Recall United States OngoingHistorical recordClass I
FDA Recall United States OngoingHistorical recordClass I
FDA Recall United States OngoingHistorical recordClass I
A map highlighting the states named in the source's distribution description.
Shading reflects state-level totals only, as published by the source. It does not imply county-level or point-level precision.
| State | Distributed |
|---|---|
| Arkansas | 1 |
| Arizona | 1 |
| California | 1 |
| Colorado | 1 |
| Florida | 1 |
| Georgia | 1 |
| Iowa | 1 |
| Illinois | 1 |
| Kansas | 1 |
| Maryland | 1 |
| North Carolina | 1 |
| New Jersey | 1 |
| Nevada | 1 |
| New York | 1 |
| Oregon | 1 |
| Rhode Island | 1 |
| Texas | 1 |
| Utah | 1 |
| Virginia | 1 |
| Washington | 1 |
States shown are extracted from the source's free-text distribution description above; a narrative description (e.g. "distributed nationwide") may not list individual states to extract.
View FDA enforcement record -- the specific openFDA record this summary was built from.
This record comes from FDA's Enforcement Report database. Not every Enforcement Report record has a separate FDA.gov recall-announcement page.
FDA Enforcement Reports -- FDA's general, official recall and enforcement information.
View raw source data -- the machine-readable record this page's information was built from.
Retrieved by Public Health Trace:
A situation in which there is a reasonable probability that use of or exposure to a product will cause serious adverse health consequences or death.
According to FDA, this recall's status is "Ongoing." Always confirm the current status using the source links below, since status can change after Public Health Trace last retrieved this record.
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