Food Recall Check
Class I · High risk Terminated Initiated Dec 18, 2013 (13 years ago)

SOLID MILK CHOCOLATE SANTA candy recall

Recalled by Concertos In Chocolate LLC · Boulder, CO, United States

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

Why it was recalled

Concertos in Chocolate LLC is recalling Solid Milk Chocolate Santa, 5oz, because the product was incorrectly labeled and has an undeclared milk allergen.

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

SOLID MILK CHOCOLATE SANTA candy

Quantity: 420

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.

ENJOY BY DATES FROM SEPTEMBER 1, 2014 THROUGH NOVEMBER 1, 2014

Where it was sold

Colorado Idaho Kansas New Mexico Utah Virginia

FDA's distribution note: COLORADO, NEW MEXICO, KANSAS, UTAH AND IDAHO; No foreign, military, government, or VA consignees.

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
Concertos In Chocolate LLC
Initiated by
Voluntary: Firm initiated
Recall initiated
Dec 18, 2013
In FDA report of
Jan 22, 2014
Terminated
Jan 26, 2016
FDA recall number
F-1404-2014 · event 67127
Official record
FDA enforcement report search

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