Class IIITerminated in FDA datasetRecall initiated Jan 27, 2017

Assorted chocolate truffles, packaged in Kraft colored boxes with the Batch PDX sticker. Boxes…

Recalling firm: Batch International Llc

Why it 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…

Historical recall record. This is not a new recall announcement. “Terminated” describes the FDA recall process; it does not certify that an individual package is safe. FDA termination date: Mar 30, 2017.

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ProductAssorted 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

No specific lot or batch information was provided in this FDA record.

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Full FDA record and distribution details

Original 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

Original FDA recall 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 details

Recall number
F-1597-2017
Event ID
76345
FDA status
Terminated
Initiated
Jan 27, 2017
Reported
Mar 22, 2017
Classified
Mar 11, 2017
Terminated
Mar 30, 2017
Quantity
Approximately 100-200 boxes
Location
Beaverton, OR, United States
Initiation type
Voluntary: Firm initiated
Notification
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit

Where it was distributed

distributed in AZ, CA, CO, IA, IL, MD, MI, NC, NJ, NV, NY, OR, and WA.

FDA source record · F-1597-2017

Data updated September 16, 2026. View official FDA data ↗

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