FDA Recall United States Terminated Historical recordClass II
Fresh Express Incorporated
- Product
- Wholesome Pantry Organic Sesame Asian Salad Kit 13 oz., UPC…
- Published
- July 22, 2020
- Distribution
- Domestic: Midwestern states of AR, CT, D…
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Policy version 2026-07-21, effective July 21, 2026.
United States
TerminatedClass II
Ready to Eat salad products containing iceberg lettuce, red cabbage and/or carrot ingredients are recalled due to a possible health risk from Cyclospora.
| Product description | UPC | Quantity | Lot / code information |
|---|---|---|---|
| Hy-Vee Greener Supreme Salad Mix 12 oz., UPC 075450120462, Iceberg lettuce, romaine lettuce, carrots & red cabbage | 075450120462 | unknown | Product Code Z160, Z161, Z163. USED BY or Before 7/11/2020 |
This recall shares FDA event ID 85918 with 10 other product entries in Public Health Trace.
FDA Recall United States Terminated Historical recordClass II
FDA Recall United States Terminated Historical recordClass II
FDA Recall United States Terminated Historical recordClass II
FDA Recall United States Terminated Historical recordClass II
FDA Recall United States Terminated Historical recordClass II
FDA Recall United States Terminated Historical recordClass II
FDA Recall United States Terminated Historical recordClass II
FDA Recall United States Terminated Historical recordClass II
FDA Recall United States Terminated Historical recordClass II
FDA Recall United States Terminated Historical recordClass II
Responsible company: Fresh Express Incorporated
FDA Recall United States Terminated Historical recordClass II
FDA Recall United States Terminated Historical recordClass II
FDA Recall United States Terminated Historical recordClass II
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 |
| Connecticut | 1 |
| District of Columbia | 1 |
| Delaware | 1 |
| Iowa | 1 |
| Illinois | 1 |
| Indiana | 1 |
| Kansas | 1 |
| Kentucky | 1 |
| Massachusetts | 1 |
| Maryland | 1 |
| Maine | 1 |
| Michigan | 1 |
| Minnesota | 1 |
| Missouri | 1 |
| Montana | 1 |
| North Carolina | 1 |
| North Dakota | 1 |
| Nebraska | 1 |
| New Hampshire | 1 |
| New Jersey | 1 |
| New York | 1 |
| Ohio | 1 |
| Oklahoma | 1 |
| Pennsylvania | 1 |
| Rhode Island | 1 |
| South Dakota | 1 |
| Tennessee | 1 |
| Virginia | 1 |
| Vermont | 1 |
| Wisconsin | 1 |
| West Virginia | 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 use of or exposure to a product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote.
According to FDA, this recall's status is "Terminated." 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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