United States
TerminatedClass I
Product samples tested positive for Listeria monocytogenes. The products also contain undeclared soy lecithin.
| Product description | UPC | Quantity | Lot / code information |
|---|---|---|---|
| Little Hatch's Spicy Queso, 13.5 oz. (382.7g) clear plastic container, Mfg. by Interstate Food Products, Lakewood, CO, littlehatches@live.com Must be Refrigerated UPC 638183961469 | 638183961469 | 280 cases of 12 - 13.5 oz. containers | 05/28, all dates. |
This recall shares FDA event ID 88038 with 3 other product entries in Public Health Trace.
FDA Recall United States TerminatedTerminated: March 11, 2022Historical recordClass I
FDA Recall United States TerminatedTerminated: March 11, 2022Historical recordClass I
FDA Recall United States TerminatedTerminated: March 11, 2022Historical recordClass I
Responsible company: Interstate Food Products, LLC
FDA Recall United States TerminatedTerminated: March 11, 2022Historical recordClass I
FDA Recall United States TerminatedTerminated: March 11, 2022Historical recordClass I
FDA Recall United States TerminatedTerminated: March 11, 2022Historical 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 |
|---|---|
| Colorado | 1 |
| Kansas | 1 |
| Missouri | 1 |
| Nebraska | 1 |
| New Mexico | 1 |
| Texas | 1 |
| Utah | 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. See FDA Enforcement Reports versus recall announcements for how that database differs from a press-release-style announcement.
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View raw source data -- the machine-readable record this page's information was built from.
Retrieved by Public Health Trace:
FDA classifies this recall as Class I. See how to read an FDA recall record (linked above) for what each classification level means.
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 responsible agency's published instructions, linked below -- recall guidance is set by that agency, not by Public Health Trace.
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This record is preserved as published by FDA, as of March 11, 2022.
Status as reported: Terminated.
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