Recall record at a glance
| Official record | F-1597-2017 |
|---|---|
| Category | Food Recalls |
| Classification | Class III |
| FDA record status | Terminated |
| Recalling firm | Batch International LLC |
| Report date | Mar 22, 2017 |
| Recall initiation date | Jan 27, 2017 |
| Quantity | Approximately 100-200 boxes |
| Location | Beaverton, OR, United States |
Official 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
Why the product was recalled
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.
Distribution information
distributed in AZ, CA, CO, IA, IL, MD, MI, NC, NJ, NV, NY, OR, and WA.
How to read the classification
FDA Class III generally covers situations in which use of or exposure to the product is not likely to cause adverse health consequences. The classification displayed here is taken from the FDA enforcement record.
Additional record details
Recall type: Voluntary: Firm initiated. Initial notification: Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit.
What to do next
If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.
About this record
Recall Lookup USA preserves the most complete source information successfully retrieved. We do not create missing facts or infer affected lots or VINs. The official record may still change, so use the identifier above when verifying current instructions.
FDA source limitation: openFDA enforcement reports are a reference dataset, not a live public-alert or recall-lifecycle service. FDA notes that enforcement-report status may not be updated after classification. Confirm current actions with the FDA, recalling firm or appropriate healthcare professional when relevant.