United States
TerminatedClass I
The firm was notified by their ingredient supplier that the pine nuts may be contaminated with Listeria monocytogenes.
| Product description | UPC | Quantity | Lot / code information |
|---|---|---|---|
| FRESH FOODS MARKET Artisan Humus Pine Nuts NET WT 10 oz (283g) | Not published in this source record | 5,082 cs/8/10 oz cups | Expiration & Lot Codes: USE BY 23 JUN 2017A W1704176, USE BY 07 JUL 2017A W1704383, USE BY 15 JUL 2017A W1705037, USE BY 20 JUL 2017A W1705122, USE BY 02 AUG 2017A W1705296 & USE BY 17 AUG 2017A W1706102 |
This recall shares FDA event ID 77587 with 2 other product entries in Public Health Trace.
FDA Recall United States TerminatedTerminated: February 22, 2018Historical recordClass I
FDA Recall United States TerminatedTerminated: February 22, 2018Historical recordClass I
Responsible company: House Of Thaller Inc
FDA Recall United States TerminatedTerminated: February 22, 2018Historical recordClass I
FDA Recall United States TerminatedTerminated: February 22, 2018Historical 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 |
| Arizona | 1 |
| California | 1 |
| Colorado | 1 |
| Connecticut | 1 |
| Florida | 1 |
| Georgia | 1 |
| Iowa | 1 |
| Idaho | 1 |
| Illinois | 1 |
| Indiana | 1 |
| Louisiana | 1 |
| Massachusetts | 1 |
| Maryland | 1 |
| Michigan | 1 |
| Minnesota | 1 |
| Missouri | 1 |
| North Carolina | 1 |
| North Dakota | 1 |
| Nebraska | 1 |
| New Jersey | 1 |
| New York | 1 |
| Ohio | 1 |
| Oklahoma | 1 |
| Oregon | 1 |
| Pennsylvania | 1 |
| South Carolina | 1 |
| Texas | 1 |
| Utah | 1 |
| Virginia | 1 |
| Washington | 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.
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.
New to reading a recall record? See how to read an FDA recall record and what recall statuses mean.
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.
Public Health Trace does not provide medical advice -- review the linked official source below for current, authoritative information.
This record is preserved as published by FDA, as of February 22, 2018.
Status as reported: Terminated.
This page does not imply a current danger or a current consumer instruction -- review the official source for the most current information.
This summary is based on the official source record referenced above. Public Health Trace does not state that any company or product is unsafe beyond what the official source has published. Read the full medical disclaimer.
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