Food Recall Check
Class I · High risk Terminated Initiated Mar 6, 2017 (10 years ago)

Dark Chocolate Coconut Bar is dark chocolate with white chocolate and coconut recall

Recalled by Dolcetta Artisan Sweets · Seattle, WA, United States

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

Why it was recalled

undeclared soy lecithin and milk

Undeclared allergens: Milk 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

Dark Chocolate Coconut Bar is dark chocolate with white chocolate and coconut, 1.2 oz (33g), product wrapped in metal foil and then wrapped in paper box.

Quantity: 300 bars

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.

none

Where it was sold

Oregon Washington

FDA's distribution note: distributed in OR and WA

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, 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
Dolcetta Artisan Sweets
Initiated by
Voluntary: Firm initiated
Recall initiated
Mar 6, 2017
In FDA report of
Apr 19, 2017
Terminated
Aug 7, 2017
FDA recall number
F-1926-2017 · event 76655
Official record
FDA enforcement report search

Also recalled with it (25 more products)

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

Showing 12 of 25.