Batch International Llc Recall: The allergens such as soy, milk, almond, coconut, hazelnut, and/or wheat are declared on an insert label inside of the assorted boxes, and not declared on the exterior of the boxes.
United States
TerminatedClass III
- Company
- Batch International Llc
- Product
- Assorted chocolate truffles, packaged in Kraft colored boxes…
- Recall date
- January 27, 2017
- Terminated
- March 30, 2017
- Source
- FDA
Reason for recall
The allergens such as soy, milk, almond, coconut, hazelnut, and/or wheat are declared on an insert label inside of the assorted boxes, and not declared on the exterior of the boxes.
- - Recall initiated
- - Reported by source
- - Recall terminated
| Product description | UPC | Quantity | Lot / code information |
|---|---|---|---|
| Assorted chocolate truffles, packaged in Kraft colored boxes with the Batch PDX sticker. Boxes contain 5, 8, 12, 18, 24 or 32 pieces with any combination of the following 14 flavors: 1. Vietnamese Iced Coffee 2. Raspberry 3. Spicy Passion 4. Bull Run Bourbon 5. Mint Meltaway 6. Almond Crisp 7. Yuzu Gimlet 8. Ghost Pepper 9. Almond n Coconut 10. Nutty Crunchy PDX 11. Earl Grey 12. Cinnamon 13. Dulce de Leche 14. Candy Cap Mushroom | Not published in this source record | Approximately 100-200 boxes | not coded |
Distribution
- distributed in AZ
- CA
- CO
- IA
- IL
- MD
- MI
- NC
- NJ
- NV
- NY
- OR
- and WA.
Official source record
- Agency
- FDA
- Dataset
- FDA Food Enforcement (Recalls)
- Recall number
- F-1597-2017
- Event ID
- 76345
- Status
- Terminated
- Classification
- Class III
- Company
- Batch International Llc
- Product description
- Assorted chocolate truffles, packaged in Kraft colored boxes with the Batch PDX sticker. Boxes contain 5, 8, 12, 18, 24 or 32 pieces with any combination of the following 14 flavors: 1. Vietnamese Iced Coffee 2. Raspberry 3. Spicy Passion 4. Bull Run Bourbon 5. Mint Meltaway 6. Almond Crisp 7. Yuzu Gimlet 8. Ghost Pepper 9. Almond n Coconut 10. Nutty Crunchy PDX 11. Earl Grey 12. Cinnamon 13. Dulce de Leche 14. Candy Cap Mushroom
- Quantity
- Approximately 100-200 boxes
- Reason
- The allergens such as soy, milk, almond, coconut, hazelnut, and/or wheat are declared on an insert label inside of the assorted boxes, and not declared on the exterior of the boxes.
- Recall initiation date
- January 27, 2017
- Report date
- March 22, 2017
- Classification date
- Not published in this source record
- Termination date
- March 30, 2017
- Distribution pattern
- distributed in AZ, CA, CO, IA, IL, MD, MI, NC, NJ, NV, NY, OR, and WA.
- UPC, lot, and code information
- not coded
- 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
Responsible company: Batch International Llc
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 |
|---|---|
| Arizona | 1 |
| California | 1 |
| Colorado | 1 |
| Iowa | 1 |
| Illinois | 1 |
| Maryland | 1 |
| Michigan | 1 |
| North Carolina | 1 |
| New Jersey | 1 |
| Nevada | 1 |
| New York | 1 |
| Oregon | 1 |
| Washington | 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 III mean?
A situation in which use of or exposure to a product is not likely to cause adverse health consequences.
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.
