Food Recall Check
Class I · High risk Terminated Initiated Dec 7, 2016 (10 years ago)

Wilbur IM10021 recall

Recalled by Cargill Cocoa & Chocolate, Inc. · Mount Joy, PA, United States

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

Why it was recalled

Cargill Cocoa & Chocolate is recalling 50 lb. cartons of Wilbur B558 Semi-Sweet Chocolate Drops because it may contain 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

Wilbur; IM10021; B558 Semisweet Chocolate Drops, 2000 CT; Net Weight 50 lb.; This item may contain dairy products; Cargill Cocoa & Chocolate, Inc., Lititz, PA 17543; BATCH 28116AANCB and 28116AANCC Material number: 100000081 packed in cardboard boxes.

Quantity: 87,900 lbs.

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.

Batch # 28116ANCB and 28116AANCC material number # 100000081

Where it was sold

Nationwide.

FDA's distribution note: Nationwide

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
Cargill Cocoa & Chocolate, Inc.
Initiated by
Voluntary: Firm initiated
Recall initiated
Dec 7, 2016
In FDA report of
Jan 4, 2017
Terminated
Sep 26, 2017
FDA recall number
F-0819-2017 · event 75893
Official record
FDA enforcement report search

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