FDA Recall United States TerminatedTerminated: November 9, 2020Historical recordClass II
Dutch Valley Food Distributors Inc.
- Product
- Dark Chocolate Almond, Net 11 oz., Contains Almond and Soy,…
- Published
- December 6, 2017
- Distribution
- Multiple states
United States
TerminatedClass II
Our supplier, GKI, did not have milk declared as an allergen on an item we repackage. Therefore our labels did not contain milk
| Product description | UPC | Quantity | Lot / code information |
|---|---|---|---|
| Dark Chocolate Cashew, Net 11 oz., Contains Cashew and Soy, Distributed By: Dutch Valley Food Distributors, Inc., Myerstown, PA 17067; UPC: 77245 00601; Lot#, Best By dates: 20160404, 04/14/17; | Not published in this source record | 19 cases 12/11 oz. bags per case | UPC: 77245 00601; Lot#, Best By dates: 20160404, 04/14/17; |
This recall shares FDA event ID 78480 with 1 other product entry in Public Health Trace.
FDA Recall United States TerminatedTerminated: November 9, 2020Historical recordClass II
Responsible company: Dutch Valley Food Distributors Inc.
FDA Recall United States TerminatedTerminated: November 9, 2020Historical recordClass II
FDA Recall United States TerminatedTerminated: January 10, 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 |
|---|---|
| Arkansas | 1 |
| Colorado | 1 |
| Connecticut | 1 |
| Delaware | 1 |
| Florida | 1 |
| Georgia | 1 |
| Illinois | 1 |
| Indiana | 1 |
| Kansas | 1 |
| Massachusetts | 1 |
| Maryland | 1 |
| Maine | 1 |
| Michigan | 1 |
| Missouri | 1 |
| Mississippi | 1 |
| North Carolina | 1 |
| New Jersey | 1 |
| New York | 1 |
| Ohio | 1 |
| Pennsylvania | 1 |
| Tennessee | 1 |
| Texas | 1 |
| Utah | 1 |
| Virginia | 1 |
| Wisconsin | 1 |
| West Virginia | 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.
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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 II. 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.
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This record is preserved as published by FDA, as of November 9, 2020.
Status as reported: Terminated.
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