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Policy version 2026-07-21, effective July 21, 2026.
United States
TerminatedClass I
Mojave Foods Corporation (subsidiary of McCormick) is initiating a voluntary recall of El Guapo Chile Habanero and Chili Pasilla-Ancho pouches due to unlabeled peanut allergen.
| Product description | UPC | Quantity | Lot / code information |
|---|---|---|---|
| El Guapo Chile Habanero Habanero Chili Pepper 0.5oz | Not published in this source record | 47,044 pouches | UPC# 044989012968; Best By Apr/05/19; Best By; Jun/21/19; Best By Jun/22/19; Best By Oct/29/19; Best By Dec/07/19; Best By Feb/05/20; Best By Feb/06/20; Best By; Jun/12/20 |
This recall shares FDA event ID 81938 with 1 other product entry in Public Health Trace.
FDA Recall United States Terminated Historical recordClass I
Responsible company: McCormick & Company, Inc. - Flavor Manufacturing Center
FDA Recall United States Terminated Historical 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 |
|---|---|
| Alabama | 1 |
| Arkansas | 1 |
| Arizona | 1 |
| California | 1 |
| Colorado | 1 |
| Florida | 1 |
| Georgia | 1 |
| Idaho | 1 |
| Illinois | 1 |
| Indiana | 1 |
| Iowa | 1 |
| Kansas | 1 |
| Kentucky | 1 |
| Michigan | 1 |
| Minnesota | 1 |
| Missouri | 1 |
| Montana | 1 |
| Nebraska | 1 |
| Nevada | 1 |
| New Mexico | 1 |
| North Carolina | 1 |
| Ohio | 1 |
| Oklahoma | 1 |
| Oregon | 1 |
| Tennessee | 1 |
| Texas | 1 |
| Utah | 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.
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.
Follow the instructions published by the responsible agency (see the source links below) -- recall guidance (e.g. dispose of the product, return it for a refund, or check for a specific lot number) varies by recall and is set by that agency, not by Public Health Trace.
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