Food Recall Check
Class III · Low risk Terminated Initiated Jan 27, 2017 (10 years ago)

Assorted chocolate truffles recall

Recalled by Batch International Llc · Beaverton, OR, United States

Class III — Low risk. Unlikely to cause harm, but violates FDA regulations.

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 boxes.

Undeclared allergens: Milk Tree nuts Soy Wheat

For someone with a food allergy the label is the only protection. An undeclared allergen can trigger a severe reaction even in a trace amount, which is why most of these recalls are Class I. All undeclared allergens recalls.

What was recalled

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

Food: Chocolate & candy

Lot codes, dates and UPCs

A recall covers only these codes. Compare them with the lot number, best-by date or UPC printed on your package.

not coded

Where it was sold

Arizona California Colorado Iowa Illinois Maryland Michigan North Carolina New Jersey Nevada New York Oregon Washington

FDA's distribution note: distributed in AZ, CA, CO, IA, IL, MD, MI, NC, NJ, NV, NY, OR, and WA.

Low risk, but check. Class III means the product is unlikely to make anyone ill but breaks an FDA rule, often a labeling one. If your package matches, the store will normally refund it. The risk from an undeclared allergen is to people allergic to milk, tree nuts, soy, wheat; for anyone else the product is generally not a safety concern. FDA lists this recall as terminated: the company has finished removing the product, so it should no longer be on shelves - but it can still be in a freezer or pantry.

Recalling firm
Batch International Llc
Initiated by
Voluntary: Firm initiated
Recall initiated
Jan 27, 2017
In FDA report of
Mar 22, 2017
Terminated
Mar 30, 2017
FDA recall number
F-1597-2017 · event 76345
Official record
FDA enforcement report search

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