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Policy version 2026-07-21, effective July 21, 2026.
United States
TerminatedClass I
Potential contamination with Listeria monocytogenes.
| Product description | UPC | Quantity | Lot / code information |
|---|---|---|---|
| UPC 8 98429 00209 1 PEACHES PRODUCE OF U.S.A. NET WT 2 LB (32 OZ) 907 g DISTRIBUTED BY MOONLIGHT PACKING CORP. REEDLEY, CALIFORNIA 93654 UPC 0 11110 18174 9 PEACHES PRODUCE OF USA NET WT 32 OZ (2 LB) 907g DISTRIBUTED BY THE KROGER CO. CINCINNATI, OHIO 45202 | Not published in this source record | 46,048 cases (12-2 lb. bags/case) | Lots: 01PCLC, 03PCAF, 106PCLF, 113PCAF, 113PCLF, 129PCLF, 134PCLF, 142PCLF, 150PCLF, 151PCLF, 159PCABA, 159PCABB, 159PCPG10, 20, 22PCAB, 22PCPG10A, 22PCPG10B, 22PCP8A, 22PCPG8B, 22PCPG8C, 23, 25, 30PCEN, 40LT, 40YP#3, 44PCLC, 44PCLCB, 45, 51PCLC, 51PCLCB, 86PCAF, 69PWPR, 79PWPRT |
This recall shares FDA event ID 97908 with 9 other product entries in Public Health Trace.
FDA Recall United States TerminatedTerminated: July 31, 2026Historical recordClass I
FDA Recall United States TerminatedTerminated: July 31, 2026Historical recordClass I
FDA Recall United States TerminatedTerminated: July 31, 2026Historical recordClass I
FDA Recall United States TerminatedTerminated: July 31, 2026Historical recordClass I
FDA Recall United States TerminatedTerminated: July 31, 2026Historical recordClass I
FDA Recall United States TerminatedTerminated: July 31, 2026Historical recordClass I
FDA Recall United States TerminatedTerminated: July 31, 2026Historical recordClass I
FDA Recall United States TerminatedTerminated: July 31, 2026Historical recordClass I
FDA Recall United States TerminatedTerminated: July 31, 2026Historical recordClass I
Responsible company: Moonlight Packing Corporation
FDA Recall United States TerminatedTerminated: July 31, 2026Historical recordClass I
FDA Recall United States TerminatedTerminated: July 31, 2026Historical recordClass I
FDA Recall United States TerminatedTerminated: July 31, 2026Historical 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 |
|---|---|
| Alabama | 1 |
| Arkansas | 1 |
| Arizona | 1 |
| California | 1 |
| Colorado | 1 |
| Connecticut | 1 |
| Florida | 1 |
| Georgia | 1 |
| Hawaii | 1 |
| Iowa | 1 |
| Illinois | 1 |
| Indiana | 1 |
| Kansas | 1 |
| Kentucky | 1 |
| Louisiana | 1 |
| Massachusetts | 1 |
| Maryland | 1 |
| Maine | 1 |
| Minnesota | 1 |
| Missouri | 1 |
| Mississippi | 1 |
| Montana | 1 |
| North Carolina | 1 |
| Nebraska | 1 |
| New Jersey | 1 |
| New Mexico | 1 |
| New York | 1 |
| Ohio | 1 |
| Oklahoma | 1 |
| Oregon | 1 |
| Pennsylvania | 1 |
| South Carolina | 1 |
| Tennessee | 1 |
| Texas | 1 |
| Utah | 1 |
| Virginia | 1 |
| Washington | 1 |
| Wisconsin | 1 |
| Wyoming | 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 "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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