Food Recall Check
Class I · High risk Terminated Initiated Apr 10, 2020 (6 years ago)

Lake Champlain CHOCOLATES recall

Recalled by Champlain Chocolate Company · Williston, VT, United States

Class I — High risk. Reasonable probability of serious harm or death.

Why it was recalled

Product contains undeclared milk.

Undeclared allergen: Milk

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

Lake Champlain CHOCOLATES, COIN DARK BULK ORG, NET WT 48 OZ (1.3 kg), APPROX 186 PIECES, INGREDIENTS: DARK CHOCOLATE (SUGAR, CHOCOLATE LIQUOR, COCOA BUTTER, COCOA POWDER (PRESSED WITH ALKALI), AND VANILLA POWDER) MAY CONTAIN TRACES OF MILK, PEANUTS, SOYBEAN, TREE NUTS, AND WHEAT

Quantity: 9 cases (1,674 pieces)

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.

Best By 11/15/21; UPC 7 69933 02301 1

Where it was sold

California Illinois Indiana New Hampshire Pennsylvania Vermont

FDA's distribution note: NH, IN, VT, CA, PA, IL

Do not eat it. Class I means FDA judged there is a reasonable probability of serious illness or death. If the brand, size and lot or date code on your package match, throw the product away or return it to the store for a refund, and clean any surface or container it touched. If anyone has eaten it and feels unwell, contact a doctor and mention the recall. The risk from an undeclared allergen is to people allergic to milk; 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
Champlain Chocolate Company
Initiated by
Voluntary: Firm initiated
Recall initiated
Apr 10, 2020
In FDA report of
Apr 29, 2020
Terminated
Aug 4, 2020
FDA recall number
F-0933-2020 · event 85455
Official record
FDA enforcement report search

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