Food Recall Check
Class I · High risk Terminated Initiated Dec 1, 2023 (3 years ago)

Manischewitz Magic Max's Dark Chocolate Coins recall

Recalled by Kenover Marketing Corp. · Bayonne, NJ, United States

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

Why it was recalled

Undeclared milk due to mispackaging

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

Manischewitz Magic Max's Dark Chocolate Coins, NET WT. 0.53 OZ (15g), UPC: 072700200387 Display Box UPC: 072700200356, 12 bags per case. Product packaged in gold foil in blue netting bags.

Quantity: 24 cases

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.

Lot 2283

Where it was sold

California Colorado Connecticut Florida Georgia Iowa Illinois Massachusetts Maryland New Hampshire New Jersey New York Oregon Pennsylvania Rhode Island South Carolina Texas Wisconsin

FDA's distribution note: Distributed to distributors and retailers in IL, PA, MD, CA, NH, RI, CO, OR, IA, FL, GA, TX, NY, NJ, SC, MA, WI and CT.

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
Kenover Marketing Corp.
Initiated by
Voluntary: Firm initiated
Recall initiated
Dec 1, 2023
In FDA report of
Dec 27, 2023
Terminated
Oct 8, 2024
FDA recall number
F-0608-2024 · event 93518
Official record
FDA enforcement report search

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