FDA Recall United States Terminated Historical recordClass I
The JM Smucker Company LLC
- Product
- JIF DARK ROAST CREMY PEANUT BUTTER packaged in 500 gram and…
- Published
- June 8, 2022
- Distribution
- Multiple states
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Policy version 2026-07-21, effective July 21, 2026.
United States
TerminatedClass I
Products are potentially contaminated with Salmonella.
| Product description | UPC | Quantity | Lot / code information |
|---|---|---|---|
| JIF NO ADDED SUGAR PEANUT BUTTER packaged in 15.5oz and 46.5oz | Not published in this source record | 115,106 cases total | Lot codes: 1274425 2140425 UPC: 5150024540, 5150041418 Best By Date: 10/01/22 - 05/20/23 |
This recall shares FDA event ID 90255 with 10 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
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: The JM Smucker Company LLC
FDA Recall United States Terminated Historical recordClass II
FDA Recall United States Terminated Historical recordClass II
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 |
|---|---|
| Alaska | 1 |
| Alabama | 1 |
| Arkansas | 1 |
| Arizona | 1 |
| California | 1 |
| Colorado | 1 |
| Connecticut | 1 |
| Delaware | 1 |
| Florida | 1 |
| Georgia | 1 |
| Hawaii | 1 |
| Iowa | 1 |
| Idaho | 1 |
| Illinois | 1 |
| Indiana | 1 |
| Kansas | 1 |
| Kentucky | 1 |
| Louisiana | 1 |
| Massachusetts | 1 |
| Maryland | 1 |
| Maine | 1 |
| Michigan | 1 |
| Minnesota | 1 |
| Missouri | 1 |
| Mississippi | 1 |
| Montana | 1 |
| North Carolina | 1 |
| North Dakota | 1 |
| Nebraska | 1 |
| New Hampshire | 1 |
| New Jersey | 1 |
| New Mexico | 1 |
| Nevada | 1 |
| New York | 1 |
| Ohio | 1 |
| Oklahoma | 1 |
| Oregon | 1 |
| Pennsylvania | 1 |
| Rhode Island | 1 |
| South Carolina | 1 |
| Tennessee | 1 |
| Texas | 1 |
| Utah | 1 |
| Virginia | 1 |
| Vermont | 1 |
| Washington | 1 |
| Wisconsin | 1 |
| West Virginia | 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.
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.
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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