FDA Recall United States Terminated Historical recordClass I
New American Food Products, LLC.
- Product
- Chocolate Premium Chocolate Treats Vanilla Caramels package…
- Published
- February 8, 2017
- Distribution
- TN
New American Food Products, LLC. Recall: Product contains peanuts undeclared allergen
United States
TerminatedClass I
- Company
- New American Food Products, LLC.
- Product
- Cumberland Farms Farmhouse Premium Chocolate Treats - Sea Sa…
- Recall date
- July 1, 2016
- Terminated
- January 19, 2017
- Source
- FDA
Reason for recall
Product contains peanuts undeclared allergen
- - Recall initiated
- - Reported by source
- - Recall terminated
| Product description | UPC | Quantity | Lot / code information |
|---|---|---|---|
| Cumberland Farms Farmhouse Premium Chocolate Treats - Sea Salt Carmel Delights, 3 oz. bag | Not published in this source record | Not published in this source record | Not published in this source record |
Distribution
- New England
Official source record
- Agency
- FDA
- Dataset
- FDA Food Enforcement (Recalls)
- Recall number
- F-1859-2016
- Status
- Terminated
- Classification
- Class I
- Company
- New American Food Products, LLC.
- Product description
- Cumberland Farms Farmhouse Premium Chocolate Treats - Sea Salt Carmel Delights, 3 oz. bag
- Quantity
- Not published in this source record
- Reason
- Product contains peanuts undeclared allergen
- Recall initiation date
- July 1, 2016
- Report date
- August 10, 2016
- Classification date
- Not published in this source record
- Termination date
- January 19, 2017
- Distribution pattern
- New England
- UPC, lot, and code information
- Not published in this source record
- Voluntary or mandated
- Not published in this source record
- Initial notification method
- Not published in this source record
- Source last updated
- Not tracked separately from the Public Health Trace retrieval date below
- Public Health Trace retrieval date
Responsible company: New American Food Products, LLC.
Other recalls from New American Food Products, LLC.
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 I mean?
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.
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.
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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?
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