Food Recall Check
Class I · High risk Terminated Initiated Nov 27, 2024 (2 years ago)

NuGo Dark Pretzel/Chocolate Chip Multipack recall

Recalled by Bazzini LLC · Allentown, PA, United States

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

Why it was recalled

The product is being recalled because of 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

NuGo Dark Pretzel/Chocolate Chip Multipack 18 ct., 50g bar, 18 bars/tray, 9 trays/case. 40case/pallet

Quantity: 511,920 bars of NuGo Dark Chocolate Pretzel/Chocolate Chocolate Chip

Food: Chocolate & candy Chips & snacks

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 Code example: B24235A Best By Date: 14 DEC 2025, 21 DEC 2025, 22 DEC 2025, 23 DEC 2025

Where it was sold

Florida Georgia Iowa Illinois Massachusetts Maryland Maine Mississippi North Carolina New Jersey Pennsylvania Virginia Washington

FDA's distribution note: The recalled product was distributed to the following states NC, MS, MA,ME, IL, PA, IA, GA, FL, MD, NJ, VA, MA, 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; 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
Bazzini LLC
Initiated by
Voluntary: Firm initiated
Recall initiated
Nov 27, 2024
In FDA report of
Feb 12, 2025
Terminated
Jul 15, 2025
FDA recall number
F-0463-2025 · event 95917
Official record
FDA enforcement report search

Also recalled with it (2 more products)

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

Other recalls by Bazzini LLC

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