FDA Recall United States Terminated Historical 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
Dutch Valley Food Distributors Inc. Recall: Our supplier, GKI, did not have milk declared as an allergen on an item we repackage. Therefore our labels did not contain milk
United States
TerminatedClass II
- Company
- Dutch Valley Food Distributors Inc.
- Product
- Dark Chocolate Cashew, Net 11 oz., Contains Cashew and Soy,…
- Recall date
- November 1, 2017
- Terminated
- November 9, 2020
- Source
- FDA
Reason for recall
Our supplier, GKI, did not have milk declared as an allergen on an item we repackage. Therefore our labels did not contain milk
- - Recall initiated
- - Reported by source
- - Recall terminated
| 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; |
Distribution
- AR
- CO
- CT
- DE
- FL
- GA
- IL
- IN
- KS
- MA
- MD
- ME
- MI
- MO
- MS
- NC
- NJ
- NY
- OH
- PA
- TN
- TX
- UT
- VA
- WI
- WV
Official source record
- Agency
- FDA
- Dataset
- FDA Food Enforcement (Recalls)
- Recall number
- F-0392-2018
- Event ID
- 78480
- Status
- Terminated
- Classification
- Class II
- Company
- Dutch Valley Food Distributors Inc.
- Product description
- 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;
- Quantity
- 19 cases 12/11 oz. bags per case
- Reason
- Our supplier, GKI, did not have milk declared as an allergen on an item we repackage. Therefore our labels did not contain milk
- Recall initiation date
- November 1, 2017
- Report date
- December 6, 2017
- Classification date
- Not published in this source record
- Termination date
- November 9, 2020
- Distribution pattern
- AR, CO, CT, DE, FL, GA, IL, IN, KS, MA, MD, ME, MI, MO, MS, NC, NJ, NY, OH, PA, TN, TX, UT, VA, WI, WV
- UPC, lot, and code information
- UPC: 77245 00601; Lot#, Best By dates: 20160404, 04/14/17;
- Voluntary or mandated
- Voluntary: Firm initiated
- Initial notification method
- Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
- Source last updated
- Not tracked separately from the Public Health Trace retrieval date below
- Public Health Trace retrieval date
Other products recalled under this same event
This recall shares FDA event ID 78480 with 1 other product entry in Public Health Trace.
Responsible company: Dutch Valley Food Distributors Inc.
Other recalls from Dutch Valley Food Distributors Inc.
FDA Recall United States Terminated Historical 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
FDA Recall United States Terminated Historical recordClass I
Dutch Valley Food Distributors Inc.
- Product
- Cappuccino Snack Mix Lot code: 20161027; Best By: 05/25/17…
- Published
- February 15, 2017
- Distribution
- DE FL GA IA ID IL IN KS MA MD…
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.
Where this information comes from
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.
Technical source data
View raw source data -- the machine-readable record this page's information was built from.
Retrieved by Public Health Trace:
Frequently asked questions
What does a Class II mean?
A situation in which use of or exposure to a product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote.
Is this recall still active?
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.
What should I do if I have this product?
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.
Where can I find more official information?
The source links below, published by FDA, are the authoritative record for this recall, including any updates issued after this summary was retrieved.
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.
