Food Recall Check
Class II · Moderate risk Terminated Initiated Feb 2, 2023 (4 years ago)

Pilgrim's Roasted Nut'Z Tri-Colored Chocolate Espresso Beans are… recall

Recalled by Pilgrims Roasted Nutz · North Plains, OR, United States

Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.

Why it was recalled

Tri-Colored Chocolate Espresso Beans product is recalled due to undeclared soy lecithin.

Undeclared allergen: Soy

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

Pilgrim's Roasted Nut'Z Tri-Colored Chocolate Espresso Beans are packaged by hand into either the 8 oz Plastic Cone Bags or 8 Oz Pouch Bags. Label declares Espresso Beans, Dark Chocolate, Milk Chocolate, Marbled White Chocolate.

Quantity: 537 packages

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.

no codes

Where it was sold

California Oregon Washington

FDA's distribution note: Distributed in California, Oregon, and Washington.

Check the codes, then return or discard. Class II means eating it may cause temporary or reversible health problems. If your package matches the recalled codes, do not eat it - return it to the store or throw it away. The risk from an undeclared allergen is to people allergic to soy; 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
Pilgrims Roasted Nutz
Initiated by
Voluntary: Firm initiated
Recall initiated
Feb 2, 2023
In FDA report of
Mar 1, 2023
Terminated
Apr 21, 2023
FDA recall number
F-0364-2023 · event 91648
Official record
FDA enforcement report search

Also recalled with it (6 more products)

FDA files each product of one recall action separately; these share the same FDA event.

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