FDA Recall United States Terminated Historical recordClass I
Reser's Fine Foods, Inc.
- Product
- Sysco Imperial Deluxe Tuna Salad, Reorder #6526826, net wt.…
- Published
- August 20, 2025
- Distribution
- Distributed in AR, CO, FL, GA, IA, IL, I…
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Policy version 2026-07-21, effective July 21, 2026.
United States
TerminatedClass I
Tuna Salad products are recalled due to potential contamination with Listeria monocytogenes because products containing Newly Weds Foods recalled Japanese Style Breadcrumbs.
| Product description | UPC | Quantity | Lot / code information |
|---|---|---|---|
| Sysco Classic Tuna Salad, Reorder #6724249, net wt. 5lb. Foodservice item. Product is packaged in clear printed plastic tub with printed lid. Keep Refrigerated. Distributed by Sysco Corporation, Houston, TX 77077 UPC on 5lb. Sysco TUB/Lid: 74865 80038 GTIN on Master Case (2/5# per case): 0071117 68049 or 10074900000000 | Not published in this source record | 779 cases | Lot 1420043323 Use By: AUG/25/25 Lot 1420046640 Use By: SEP/1/25 |
This recall shares FDA event ID 97283 with 6 other product entries in Public Health Trace.
FDA Recall United States Terminated Historical recordClass I
FDA Recall United States Terminated Historical recordClass I
FDA Recall United States Terminated Historical recordClass I
FDA Recall United States Terminated Historical recordClass I
FDA Recall United States Terminated Historical recordClass I
FDA Recall United States Terminated Historical recordClass I
Responsible company: Reser's Fine Foods, Inc.
FDA Recall United States Terminated 2026 recordClass I
FDA Recall United States Terminated Historical recordClass I
FDA Recall United States Terminated Historical 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 |
| Colorado | 1 |
| Florida | 1 |
| Georgia | 1 |
| Iowa | 1 |
| Illinois | 1 |
| Indiana | 1 |
| Kansas | 1 |
| Kentucky | 1 |
| Louisiana | 1 |
| Massachusetts | 1 |
| Maryland | 1 |
| Michigan | 1 |
| Minnesota | 1 |
| Missouri | 1 |
| Mississippi | 1 |
| North Dakota | 1 |
| Nebraska | 1 |
| New Hampshire | 1 |
| New Jersey | 1 |
| New Mexico | 1 |
| New York | 1 |
| Ohio | 1 |
| Oklahoma | 1 |
| Pennsylvania | 1 |
| Tennessee | 1 |
| Texas | 1 |
| Virginia | 1 |
| Wisconsin | 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.
No separate FDA public notice was found for this enforcement record. The information below comes from FDA's Recall Enterprise System through openFDA.
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.
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